Canonical Allele Identifier: CA6988807

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944246C>T , CM000675.2:g.51944246C>T	GRCh38
NC_000013.10:g.52518382C>T , CM000675.1:g.52518382C>T	GRCh37
NC_000013.9:g.51416383C>T	NCBI36
NG_008806.1:g.72249G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1692G>A	ENSP00000489512.2:n.*894-1692G>A
ENST00000673864.2:c.*1850G>A	ENSP00000501045.2:n.*1850G>A
ENST00000674147.2:c.2485G>A	ENSP00000500964.2:p.Val829Ile
ENST00000242839.10:c.3106G>A MANE Select	ENSP00000242839.5:p.Val1036Ile
ENST00000344297.9:c.2485G>A	ENSP00000342559.5:p.Val829Ile
ENST00000400366.6:c.2773G>A	ENSP00000383217.3:p.Val925Ile
ENST00000448424.7:c.2854G>A	ENSP00000416738.3:p.Val952Ile
ENST00000673772.1:c.2872G>A	ENSP00000501168.1:p.Val958Ile
ENST00000673867.1:n.3245G>A
ENST00000674126.1:n.3469G>A
ENST00000674147.1:c.2041G>A	ENSP00000500964.1:p.Val681Ile
ENST00000242839.8:c.3106G>A	ENSP00000242839.4:p.Val1036Ile
ENST00000344297.8:c.2485G>A	ENSP00000342559.5:p.Val829Ile
ENST00000400366.5:c.2773G>A	ENSP00000383217.3:p.Val925Ile
ENST00000400370.8:c.1816G>A	ENSP00000383221.3:p.Val606Ile
ENST00000418097.7:c.2911G>A	ENSP00000393343.2:p.Val971Ile
ENST00000448424.6:c.2872G>A	ENSP00000416738.2:p.Val958Ile
ENST00000466629.1:n.326G>A
ENST00000634296.1:c.1022-1692G>A
ENST00000634308.1:c.*207G>A	ENSP00000489234.1:n.*207G>A
ENST00000634620.1:n.3850G>A
ENST00000634810.1:n.2451G>A
ENST00000634844.1:c.2962G>A	ENSP00000489398.1:p.Val988Ile
ENST00000635406.1:n.452G>A
NM_000053.3:c.3106G>A	NP_000044.2:p.Val1036Ile
NM_001005918.2:c.2485G>A	NP_001005918.1:p.Val829Ile
NM_001243182.1:c.2773G>A	NP_001230111.1:p.Val925Ile
XM_005266423.2:c.3010G>A	XP_005266480.1:p.Val1004Ile
XM_005266424.3:c.3010G>A	XP_005266481.1:p.Val1004Ile
XM_005266427.2:c.2872G>A	XP_005266484.1:p.Val958Ile
XM_005266428.1:c.2854G>A	XP_005266485.1:p.Val952Ile
XM_005266430.3:c.3106G>A	XP_005266487.1:p.Val1036Ile
XM_005266431.2:c.3070G>A	XP_005266488.1:p.Val1024Ile
XM_005266432.2:c.2620G>A	XP_005266489.1:p.Val874Ile
XM_006719837.2:c.3010G>A	XP_006719900.1:p.Val1004Ile
XM_006719838.1:c.922G>A	XP_006719901.1:p.Val308Ile
XM_006719839.1:c.877-1692G>A	XP_006719902.1:n.877-1692G>A
XM_011535117.1:c.3010G>A	XP_011533419.1:p.Val1004Ile
XM_011535118.1:c.2971G>A	XP_011533420.1:p.Val991Ile
XM_011535119.1:c.3061-1692G>A	XP_011533421.1:n.3061-1692G>A
XM_011535120.1:c.2692G>A	XP_011533422.1:p.Val898Ile
XM_011535121.1:c.2731-1692G>A	XP_011533423.1:n.2731-1692G>A
XM_011535122.1:c.1774G>A	XP_011533424.1:p.Val592Ile
XR_941601.1:n.3325G>A
XR_941602.1:n.3325G>A
XR_941603.1:n.3325G>A
XR_941604.1:n.3325G>A
NM_001330578.1:c.2872G>A	NP_001317507.1:p.Val958Ile
NM_001330579.1:c.2854G>A	NP_001317508.1:p.Val952Ile
XM_005266424.4:c.3010G>A	XP_005266481.1:p.Val1004Ile
XM_005266430.4:c.3106G>A	XP_005266487.1:p.Val1036Ile
XM_005266431.4:c.3070G>A	XP_005266488.1:p.Val1024Ile
XM_006719837.3:c.3010G>A	XP_006719900.1:p.Val1004Ile
XM_011535117.3:c.3010G>A	XP_011533419.1:p.Val1004Ile
XM_017020627.1:c.3010G>A	XP_016876116.1:p.Val1004Ile
NM_000053.4:c.3106G>A MANE Select	NP_000044.2:p.Val1036Ile
NM_001005918.3:c.2485G>A	NP_001005918.1:p.Val829Ile
NM_001330579.2:c.2854G>A	NP_001317508.1:p.Val952Ile
NM_001243182.2:c.2773G>A	NP_001230111.1:p.Val925Ile
NM_001330578.2:c.2872G>A	NP_001317507.1:p.Val958Ile