Canonical Allele Identifier: CA388024564

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52513303C>A (hg19) ; chr13:g.51939167C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51939167C>A , CM000675.2:g.51939167C>A	GRCh38
NC_000013.10:g.52513303C>A , CM000675.1:g.52513303C>A	GRCh37
NC_000013.9:g.51411304C>A	NCBI36
NG_008806.1:g.77328G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1233G>T	ENSP00000489512.2:n.*1233G>T
ENST00000673864.2:c.*2327G>T	ENSP00000501045.2:n.*2327G>T
ENST00000674147.2:c.2962G>T	ENSP00000500964.2:p.Ala988Ser
ENST00000242839.10:c.3583G>T MANE Select	ENSP00000242839.5:p.Ala1195Ser
ENST00000344297.9:c.2962G>T	ENSP00000342559.5:p.Ala988Ser
ENST00000400366.6:c.3250G>T	ENSP00000383217.3:p.Ala1084Ser
ENST00000448424.7:c.3331G>T	ENSP00000416738.3:p.Ala1111Ser
ENST00000673696.1:n.824G>T
ENST00000673772.1:c.3349G>T	ENSP00000501168.1:p.Ala1117Ser
ENST00000673867.1:n.3722G>T
ENST00000673923.1:n.449G>T
ENST00000674147.1:c.2518G>T	ENSP00000500964.1:p.Ala840Ser
ENST00000242839.8:c.3583G>T	ENSP00000242839.4:p.Ala1195Ser
ENST00000344297.8:c.2962G>T	ENSP00000342559.5:p.Ala988Ser
ENST00000400366.5:c.3250G>T	ENSP00000383217.3:p.Ala1084Ser
ENST00000400370.8:c.2293G>T	ENSP00000383221.3:p.Ala765Ser
ENST00000418097.7:c.3388G>T	ENSP00000393343.2:p.Ala1130Ser
ENST00000448424.6:c.3349G>T	ENSP00000416738.2:p.Ala1117Ser
ENST00000634296.1:c.1361G>T
ENST00000634308.1:c.*684G>T	ENSP00000489234.1:n.*684G>T
ENST00000634620.1:n.4327G>T
ENST00000634810.1:n.2928G>T
ENST00000634844.1:c.3439G>T	ENSP00000489398.1:p.Ala1147Ser
NM_000053.3:c.3583G>T	NP_000044.2:p.Ala1195Ser
NM_001005918.2:c.2962G>T	NP_001005918.1:p.Ala988Ser
NM_001243182.1:c.3250G>T	NP_001230111.1:p.Ala1084Ser
XM_005266423.2:c.3487G>T	XP_005266480.1:p.Ala1163Ser
XM_005266424.3:c.3487G>T	XP_005266481.1:p.Ala1163Ser
XM_005266427.2:c.3349G>T	XP_005266484.1:p.Ala1117Ser
XM_005266428.1:c.3331G>T	XP_005266485.1:p.Ala1111Ser
XM_005266430.3:c.3583G>T	XP_005266487.1:p.Ala1195Ser
XM_005266431.2:c.3547G>T	XP_005266488.1:p.Ala1183Ser
XM_005266432.2:c.3097G>T	XP_005266489.1:p.Ala1033Ser
XM_006719837.2:c.3487G>T	XP_006719900.1:p.Ala1163Ser
XM_006719838.1:c.1399G>T	XP_006719901.1:p.Ala467Ser
XM_006719839.1:c.1216G>T	XP_006719902.1:p.Ala406Ser
XM_011535117.1:c.3487G>T	XP_011533419.1:p.Ala1163Ser
XM_011535118.1:c.3448G>T	XP_011533420.1:p.Ala1150Ser
XM_011535119.1:c.3400G>T	XP_011533421.1:p.Ala1134Ser
XM_011535120.1:c.3169G>T	XP_011533422.1:p.Ala1057Ser
XM_011535121.1:c.3070G>T	XP_011533423.1:p.Ala1024Ser
XM_011535122.1:c.2251G>T	XP_011533424.1:p.Ala751Ser
XR_941601.1:n.3802G>T
XR_941602.1:n.3802G>T
XR_941603.1:n.3802G>T
XR_941604.1:n.3802G>T
NM_001330578.1:c.3349G>T	NP_001317507.1:p.Ala1117Ser
NM_001330579.1:c.3331G>T	NP_001317508.1:p.Ala1111Ser
XM_005266424.4:c.3487G>T	XP_005266481.1:p.Ala1163Ser
XM_005266430.4:c.3583G>T	XP_005266487.1:p.Ala1195Ser
XM_005266431.4:c.3547G>T	XP_005266488.1:p.Ala1183Ser
XM_006719837.3:c.3487G>T	XP_006719900.1:p.Ala1163Ser
XM_011535117.3:c.3487G>T	XP_011533419.1:p.Ala1163Ser
XM_017020627.1:c.3487G>T	XP_016876116.1:p.Ala1163Ser
NM_000053.4:c.3583G>T MANE Select	NP_000044.2:p.Ala1195Ser
NM_001005918.3:c.2962G>T	NP_001005918.1:p.Ala988Ser
NM_001330579.2:c.3331G>T	NP_001317508.1:p.Ala1111Ser
NM_001243182.2:c.3250G>T	NP_001230111.1:p.Ala1084Ser
NM_001330578.2:c.3349G>T	NP_001317507.1:p.Ala1117Ser