Canonical Allele Identifier: CA388015392

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 2682332
• ClinVar RCV Id: RCV003479705
• MyVariant Identifiers: chr13:g.52524292C>T (hg19) ; chr13:g.51950156C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51950156C>T , CM000675.2:g.51950156C>T	GRCh38
NC_000013.10:g.52524292C>T , CM000675.1:g.52524292C>T	GRCh37
NC_000013.9:g.51422293C>T	NCBI36
NG_008806.1:g.66339G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*414G>A	ENSP00000489512.2:n.*414G>A
ENST00000673864.2:c.*1325G>A	ENSP00000501045.2:n.*1325G>A
ENST00000674147.2:c.2095G>A	ENSP00000500964.2:p.Ala699Thr
ENST00000242839.10:c.2581G>A MANE Select	ENSP00000242839.5:p.Ala861Thr
ENST00000344297.9:c.2095G>A	ENSP00000342559.5:p.Ala699Thr
ENST00000400366.6:c.2248G>A	ENSP00000383217.3:p.Ala750Thr
ENST00000448424.7:c.2329G>A	ENSP00000416738.3:p.Ala777Thr
ENST00000673772.1:c.2347G>A	ENSP00000501168.1:p.Ala783Thr
ENST00000674147.1:c.1651G>A	ENSP00000500964.1:p.Ala551Thr
ENST00000242839.8:c.2581G>A	ENSP00000242839.4:p.Ala861Thr
ENST00000344297.8:c.2095G>A	ENSP00000342559.5:p.Ala699Thr
ENST00000400366.5:c.2248G>A	ENSP00000383217.3:p.Ala750Thr
ENST00000400370.8:c.1291G>A	ENSP00000383221.3:p.Ala431Thr
ENST00000418097.7:c.2581G>A	ENSP00000393343.2:p.Ala861Thr
ENST00000448424.6:c.2347G>A	ENSP00000416738.2:p.Ala783Thr
ENST00000634296.1:c.542G>A
ENST00000634308.1:c.2347G>A	ENSP00000489234.1:p.Ala783Thr
ENST00000634620.1:n.3379G>A
ENST00000634810.1:n.1926G>A
ENST00000634844.1:c.2437G>A	ENSP00000489398.1:p.Ala813Thr
ENST00000635406.1:n.212-3678G>A
NM_000053.3:c.2581G>A	NP_000044.2:p.Ala861Thr
NM_001005918.2:c.2095G>A	NP_001005918.1:p.Ala699Thr
NM_001243182.1:c.2248G>A	NP_001230111.1:p.Ala750Thr
XM_005266423.2:c.2485G>A	XP_005266480.1:p.Ala829Thr
XM_005266424.3:c.2485G>A	XP_005266481.1:p.Ala829Thr
XM_005266427.2:c.2347G>A	XP_005266484.1:p.Ala783Thr
XM_005266428.1:c.2329G>A	XP_005266485.1:p.Ala777Thr
XM_005266430.3:c.2581G>A	XP_005266487.1:p.Ala861Thr
XM_005266431.2:c.2545G>A	XP_005266488.1:p.Ala849Thr
XM_005266432.2:c.2095G>A	XP_005266489.1:p.Ala699Thr
XM_006719837.2:c.2485G>A	XP_006719900.1:p.Ala829Thr
XM_006719838.1:c.397G>A	XP_006719901.1:p.Ala133Thr
XM_006719839.1:c.397G>A	XP_006719902.1:p.Ala133Thr
XM_011535117.1:c.2485G>A	XP_011533419.1:p.Ala829Thr
XM_011535118.1:c.2581G>A	XP_011533420.1:p.Ala861Thr
XM_011535119.1:c.2581G>A	XP_011533421.1:p.Ala861Thr
XM_011535120.1:c.2167G>A	XP_011533422.1:p.Ala723Thr
XM_011535121.1:c.2581G>A	XP_011533423.1:p.Ala861Thr
XM_011535122.1:c.1249G>A	XP_011533424.1:p.Ala417Thr
XR_941601.1:n.2800G>A
XR_941602.1:n.2800G>A
XR_941603.1:n.2800G>A
XR_941604.1:n.2800G>A
NM_001330578.1:c.2347G>A	NP_001317507.1:p.Ala783Thr
NM_001330579.1:c.2329G>A	NP_001317508.1:p.Ala777Thr
XM_005266424.4:c.2485G>A	XP_005266481.1:p.Ala829Thr
XM_005266430.4:c.2581G>A	XP_005266487.1:p.Ala861Thr
XM_005266431.4:c.2545G>A	XP_005266488.1:p.Ala849Thr
XM_006719837.3:c.2485G>A	XP_006719900.1:p.Ala829Thr
XM_011535117.3:c.2485G>A	XP_011533419.1:p.Ala829Thr
XM_017020627.1:c.2485G>A	XP_016876116.1:p.Ala829Thr
NM_000053.4:c.2581G>A MANE Select	NP_000044.2:p.Ala861Thr
NM_001005918.3:c.2095G>A	NP_001005918.1:p.Ala699Thr
NM_001330579.2:c.2329G>A	NP_001317508.1:p.Ala777Thr
NM_001243182.2:c.2248G>A	NP_001230111.1:p.Ala750Thr
NM_001330578.2:c.2347G>A	NP_001317507.1:p.Ala783Thr