Canonical Allele Identifier: CA484024253

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52511509C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51937373C>G , CM000675.2:g.51937373C>G	GRCh38
NC_000013.10:g.52511509C>G , CM000675.1:g.52511509C>G	GRCh37
NC_000013.9:g.51409510C>G	NCBI36
NG_008806.1:g.79122G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*1574G>C	ENSP00000489512.2:n.*1574G>C
ENST00000673864.2:c.*2668G>C	ENSP00000501045.2:n.*2668G>C
ENST00000674147.2:c.3303G>C	ENSP00000500964.2:p.Val1101=
ENST00000242839.10:c.3924G>C MANE Select	ENSP00000242839.5:p.Val1308=
ENST00000344297.9:c.3303G>C	ENSP00000342559.5:p.Val1101=
ENST00000400366.6:c.3591G>C	ENSP00000383217.3:p.Val1197=
ENST00000448424.7:c.3672G>C	ENSP00000416738.3:p.Val1224=
ENST00000673696.1:n.1247G>C
ENST00000673772.1:c.3690G>C	ENSP00000501168.1:p.Val1230=
ENST00000673867.1:n.4063G>C
ENST00000673923.1:n.790G>C
ENST00000674147.1:c.2859G>C	ENSP00000500964.1:p.Val953=
ENST00000242839.8:c.3924G>C	ENSP00000242839.4:p.Val1308=
ENST00000344297.8:c.3303G>C	ENSP00000342559.5:p.Val1101=
ENST00000400366.5:c.3591G>C	ENSP00000383217.3:p.Val1197=
ENST00000400370.8:c.2634G>C	ENSP00000383221.3:p.Val878=
ENST00000418097.7:c.3729G>C	ENSP00000393343.2:p.Val1243=
ENST00000448424.6:c.3690G>C	ENSP00000416738.2:p.Val1230=
ENST00000634296.1:c.1702G>C
ENST00000634308.1:c.*1025G>C	ENSP00000489234.1:n.*1025G>C
ENST00000634620.1:n.4668G>C
ENST00000634810.1:n.3269G>C
ENST00000634844.1:c.3780G>C	ENSP00000489398.1:p.Val1260=
NM_000053.3:c.3924G>C	NP_000044.2:p.Val1308=
NM_001005918.2:c.3303G>C	NP_001005918.1:p.Val1101=
NM_001243182.1:c.3591G>C	NP_001230111.1:p.Val1197=
XM_005266423.2:c.3828G>C	XP_005266480.1:p.Val1276=
XM_005266424.3:c.3828G>C	XP_005266481.1:p.Val1276=
XM_005266427.2:c.3690G>C	XP_005266484.1:p.Val1230=
XM_005266428.1:c.3672G>C	XP_005266485.1:p.Val1224=
XM_005266430.3:c.3924G>C	XP_005266487.1:p.Val1308=
XM_005266431.2:c.3888G>C	XP_005266488.1:p.Val1296=
XM_005266432.2:c.3438G>C	XP_005266489.1:p.Val1146=
XM_006719837.2:c.3828G>C	XP_006719900.1:p.Val1276=
XM_006719838.1:c.1740G>C	XP_006719901.1:p.Val580=
XM_006719839.1:c.1557G>C	XP_006719902.1:p.Val519=
XM_011535117.1:c.3828G>C	XP_011533419.1:p.Val1276=
XM_011535118.1:c.3789G>C	XP_011533420.1:p.Val1263=
XM_011535119.1:c.3741G>C	XP_011533421.1:p.Val1247=
XM_011535120.1:c.3510G>C	XP_011533422.1:p.Val1170=
XM_011535121.1:c.3411G>C	XP_011533423.1:p.Val1137=
XM_011535122.1:c.2592G>C	XP_011533424.1:p.Val864=
XR_941601.1:n.4143G>C
XR_941602.1:n.4143G>C
XR_941603.1:n.4143G>C
XR_941604.1:n.4143G>C
NM_001330578.1:c.3690G>C	NP_001317507.1:p.Val1230=
NM_001330579.1:c.3672G>C	NP_001317508.1:p.Val1224=
XM_005266424.4:c.3828G>C	XP_005266481.1:p.Val1276=
XM_005266430.4:c.3924G>C	XP_005266487.1:p.Val1308=
XM_005266431.4:c.3888G>C	XP_005266488.1:p.Val1296=
XM_006719837.3:c.3828G>C	XP_006719900.1:p.Val1276=
XM_011535117.3:c.3828G>C	XP_011533419.1:p.Val1276=
XM_017020627.1:c.3828G>C	XP_016876116.1:p.Val1276=
NM_000053.4:c.3924G>C MANE Select	NP_000044.2:p.Val1308=
NM_001005918.3:c.3303G>C	NP_001005918.1:p.Val1101=
NM_001330579.2:c.3672G>C	NP_001317508.1:p.Val1224=
NM_001243182.2:c.3591G>C	NP_001230111.1:p.Val1197=
NM_001330578.2:c.3690G>C	NP_001317507.1:p.Val1230=