Canonical Allele Identifier: CA2091553239
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51937243_51937244delinsGC , CM000675.2:g.51937243_51937244delinsGC GRCh38
NC_000013.10:g.52511379_52511380delinsGC , CM000675.1:g.52511379_52511380delinsGC GRCh37
NC_000013.9:g.51409380_51409381delinsGC NCBI36
NG_008806.1:g.79251_79252delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000634296.2:c.*1671+32_*1671+33delinsGC ENSP00000489512.2:n.*1671+32_*1671+33deli...
ENST00000673864.2:c.*2765+32_*2765+33delinsGC ENSP00000501045.2:n.*2765+32_*2765+33deli...
ENST00000674147.2:c.3400+32_3400+33delinsGC ENSP00000500964.2:n.3400+32_3400+33delins...
ENST00000242839.10:c.4021+32_4021+33delinsGC MANE Select ENSP00000242839.5:n.4021+32_4021+33delins...
ENST00000344297.9:c.3400+32_3400+33delinsGC ENSP00000342559.5:n.3400+32_3400+33delins...
ENST00000400366.6:c.3688+32_3688+33delinsGC ENSP00000383217.3:n.3688+32_3688+33delins...
ENST00000448424.7:c.3769+32_3769+33delinsGC ENSP00000416738.3:n.3769+32_3769+33delins...
ENST00000673696.1:n.1344+32_1344+33delinsGC
ENST00000673772.1:c.3787+32_3787+33delinsGC ENSP00000501168.1:n.3787+32_3787+33delins...
ENST00000673867.1:n.4160+32_4160+33delinsGC
ENST00000673923.1:n.887+32_887+33delinsGC
ENST00000674147.1:c.2956+32_2956+33delinsGC ENSP00000500964.1:n.2956+32_2956+33delins...
ENST00000242839.8:c.4021+32_4021+33delinsGC ENSP00000242839.4:n.4021+32_4021+33delins...
ENST00000344297.8:c.3400+32_3400+33delinsGC ENSP00000342559.5:n.3400+32_3400+33delins...
ENST00000400366.5:c.3688+32_3688+33delinsGC ENSP00000383217.3:n.3688+32_3688+33delins...
ENST00000400370.8:c.2731+32_2731+33delinsGC ENSP00000383221.3:n.2731+32_2731+33delins...
ENST00000418097.7:c.3826+32_3826+33delinsGC ENSP00000393343.2:n.3826+32_3826+33delins...
ENST00000448424.6:c.3787+32_3787+33delinsGC ENSP00000416738.2:n.3787+32_3787+33delins...
ENST00000634296.1:c.1799+32_1799+33delinsGC
ENST00000634308.1:c.*1122+32_*1122+33delinsGC ENSP00000489234.1:n.*1122+32_*1122+33deli...
ENST00000634620.1:n.4765+32_4765+33delinsGC
ENST00000634810.1:n.3366+32_3366+33delinsGC
ENST00000634844.1:c.3877+32_3877+33delinsGC ENSP00000489398.1:n.3877+32_3877+33delins...
NM_000053.3:c.4021+32_4021+33delinsGC NP_000044.2:n.4021+32_4021+33delinsGC
NM_001005918.2:c.3400+32_3400+33delinsGC NP_001005918.1:n.3400+32_3400+33delinsGC
NM_001243182.1:c.3688+32_3688+33delinsGC NP_001230111.1:n.3688+32_3688+33delinsGC
XM_005266423.2:c.3925+32_3925+33delinsGC XP_005266480.1:n.3925+32_3925+33delinsGC
XM_005266424.3:c.3925+32_3925+33delinsGC XP_005266481.1:n.3925+32_3925+33delinsGC
XM_005266427.2:c.3787+32_3787+33delinsGC XP_005266484.1:n.3787+32_3787+33delinsGC
XM_005266428.1:c.3769+32_3769+33delinsGC XP_005266485.1:n.3769+32_3769+33delinsGC
XM_005266430.3:c.4021+32_4021+33delinsGC XP_005266487.1:n.4021+32_4021+33delinsGC
XM_005266431.2:c.3985+32_3985+33delinsGC XP_005266488.1:n.3985+32_3985+33delinsGC
XM_005266432.2:c.3535+32_3535+33delinsGC XP_005266489.1:n.3535+32_3535+33delinsGC
XM_006719837.2:c.3925+32_3925+33delinsGC XP_006719900.1:n.3925+32_3925+33delinsGC
XM_006719838.1:c.1837+32_1837+33delinsGC XP_006719901.1:n.1837+32_1837+33delinsGC
XM_006719839.1:c.1654+32_1654+33delinsGC XP_006719902.1:n.1654+32_1654+33delinsGC
XM_011535117.1:c.3925+32_3925+33delinsGC XP_011533419.1:n.3925+32_3925+33delinsGC
XM_011535118.1:c.3886+32_3886+33delinsGC XP_011533420.1:n.3886+32_3886+33delinsGC
XM_011535119.1:c.3838+32_3838+33delinsGC XP_011533421.1:n.3838+32_3838+33delinsGC
XM_011535120.1:c.3607+32_3607+33delinsGC XP_011533422.1:n.3607+32_3607+33delinsGC
XM_011535121.1:c.3508+32_3508+33delinsGC XP_011533423.1:n.3508+32_3508+33delinsGC
XM_011535122.1:c.2689+32_2689+33delinsGC XP_011533424.1:n.2689+32_2689+33delinsGC
XR_941601.1:n.4240+32_4240+33delinsGC
XR_941602.1:n.4240+32_4240+33delinsGC
XR_941603.1:n.4240+32_4240+33delinsGC
XR_941604.1:n.4240+32_4240+33delinsGC
NM_001330578.1:c.3787+32_3787+33delinsGC NP_001317507.1:n.3787+32_3787+33delinsGC
NM_001330579.1:c.3769+32_3769+33delinsGC NP_001317508.1:n.3769+32_3769+33delinsGC
XM_005266424.4:c.3925+32_3925+33delinsGC XP_005266481.1:n.3925+32_3925+33delinsGC
XM_005266430.4:c.4021+32_4021+33delinsGC XP_005266487.1:n.4021+32_4021+33delinsGC
XM_005266431.4:c.3985+32_3985+33delinsGC XP_005266488.1:n.3985+32_3985+33delinsGC
XM_006719837.3:c.3925+32_3925+33delinsGC XP_006719900.1:n.3925+32_3925+33delinsGC
XM_011535117.3:c.3925+32_3925+33delinsGC XP_011533419.1:n.3925+32_3925+33delinsGC
XM_017020627.1:c.3925+32_3925+33delinsGC XP_016876116.1:n.3925+32_3925+33delinsGC
NM_000053.4:c.4021+32_4021+33delinsGC MANE Select NP_000044.2:n.4021+32_4021+33delinsGC
NM_001005918.3:c.3400+32_3400+33delinsGC NP_001005918.1:n.3400+32_3400+33delinsGC
NM_001330579.2:c.3769+32_3769+33delinsGC NP_001317508.1:n.3769+32_3769+33delinsGC
NM_001243182.2:c.3688+32_3688+33delinsGC NP_001230111.1:n.3688+32_3688+33delinsGC
NM_001330578.2:c.3787+32_3787+33delinsGC NP_001317507.1:n.3787+32_3787+33delinsGC