Canonical Allele Identifier: CA2623118840

Gene: ATP7B

Linked Data

• gnomAD v4: 13-51937135-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51937135A>G , CM000675.2:g.51937135A>G	GRCh38
NC_000013.10:g.52511271A>G , CM000675.1:g.52511271A>G	GRCh37
NC_000013.9:g.51409272A>G	NCBI36
NG_008806.1:g.79360T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1671+141T>C	ENSP00000489512.2:n.*1671+141T>C
ENST00000673864.2:c.*2765+141T>C	ENSP00000501045.2:n.*2765+141T>C
ENST00000674147.2:c.3400+141T>C	ENSP00000500964.2:n.3400+141T>C
ENST00000242839.10:c.4021+141T>C MANE Select	ENSP00000242839.5:n.4021+141T>C
ENST00000344297.9:c.3400+141T>C	ENSP00000342559.5:n.3400+141T>C
ENST00000400366.6:c.3688+141T>C	ENSP00000383217.3:n.3688+141T>C
ENST00000448424.7:c.3769+141T>C	ENSP00000416738.3:n.3769+141T>C
ENST00000673696.1:n.1344+141T>C
ENST00000673772.1:c.3787+141T>C	ENSP00000501168.1:n.3787+141T>C
ENST00000673867.1:n.4160+141T>C
ENST00000673923.1:n.887+141T>C
ENST00000674147.1:c.2956+141T>C	ENSP00000500964.1:n.2956+141T>C
ENST00000242839.8:c.4021+141T>C	ENSP00000242839.4:n.4021+141T>C
ENST00000344297.8:c.3400+141T>C	ENSP00000342559.5:n.3400+141T>C
ENST00000400366.5:c.3688+141T>C	ENSP00000383217.3:n.3688+141T>C
ENST00000400370.8:c.2731+141T>C	ENSP00000383221.3:n.2731+141T>C
ENST00000418097.7:c.3826+141T>C	ENSP00000393343.2:n.3826+141T>C
ENST00000448424.6:c.3787+141T>C	ENSP00000416738.2:n.3787+141T>C
ENST00000634296.1:c.1799+141T>C
ENST00000634308.1:c.*1122+141T>C	ENSP00000489234.1:n.*1122+141T>C
ENST00000634620.1:n.4765+141T>C
ENST00000634810.1:n.3366+141T>C
ENST00000634844.1:c.3877+141T>C	ENSP00000489398.1:n.3877+141T>C
NM_000053.3:c.4021+141T>C	NP_000044.2:n.4021+141T>C
NM_001005918.2:c.3400+141T>C	NP_001005918.1:n.3400+141T>C
NM_001243182.1:c.3688+141T>C	NP_001230111.1:n.3688+141T>C
XM_005266423.2:c.3925+141T>C	XP_005266480.1:n.3925+141T>C
XM_005266424.3:c.3925+141T>C	XP_005266481.1:n.3925+141T>C
XM_005266427.2:c.3787+141T>C	XP_005266484.1:n.3787+141T>C
XM_005266428.1:c.3769+141T>C	XP_005266485.1:n.3769+141T>C
XM_005266430.3:c.4021+141T>C	XP_005266487.1:n.4021+141T>C
XM_005266431.2:c.3985+141T>C	XP_005266488.1:n.3985+141T>C
XM_005266432.2:c.3535+141T>C	XP_005266489.1:n.3535+141T>C
XM_006719837.2:c.3925+141T>C	XP_006719900.1:n.3925+141T>C
XM_006719838.1:c.1837+141T>C	XP_006719901.1:n.1837+141T>C
XM_006719839.1:c.1654+141T>C	XP_006719902.1:n.1654+141T>C
XM_011535117.1:c.3925+141T>C	XP_011533419.1:n.3925+141T>C
XM_011535118.1:c.3886+141T>C	XP_011533420.1:n.3886+141T>C
XM_011535119.1:c.3838+141T>C	XP_011533421.1:n.3838+141T>C
XM_011535120.1:c.3607+141T>C	XP_011533422.1:n.3607+141T>C
XM_011535121.1:c.3508+141T>C	XP_011533423.1:n.3508+141T>C
XM_011535122.1:c.2689+141T>C	XP_011533424.1:n.2689+141T>C
XR_941601.1:n.4240+141T>C
XR_941602.1:n.4240+141T>C
XR_941603.1:n.4240+141T>C
XR_941604.1:n.4240+141T>C
NM_001330578.1:c.3787+141T>C	NP_001317507.1:n.3787+141T>C
NM_001330579.1:c.3769+141T>C	NP_001317508.1:n.3769+141T>C
XM_005266424.4:c.3925+141T>C	XP_005266481.1:n.3925+141T>C
XM_005266430.4:c.4021+141T>C	XP_005266487.1:n.4021+141T>C
XM_005266431.4:c.3985+141T>C	XP_005266488.1:n.3985+141T>C
XM_006719837.3:c.3925+141T>C	XP_006719900.1:n.3925+141T>C
XM_011535117.3:c.3925+141T>C	XP_011533419.1:n.3925+141T>C
XM_017020627.1:c.3925+141T>C	XP_016876116.1:n.3925+141T>C
NM_000053.4:c.4021+141T>C MANE Select	NP_000044.2:n.4021+141T>C
NM_001005918.3:c.3400+141T>C	NP_001005918.1:n.3400+141T>C
NM_001330579.2:c.3769+141T>C	NP_001317508.1:n.3769+141T>C
NM_001243182.2:c.3688+141T>C	NP_001230111.1:n.3688+141T>C
NM_001330578.2:c.3787+141T>C	NP_001317507.1:n.3787+141T>C