Canonical Allele Identifier: CA484024390

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52524203C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51950067C>G , CM000675.2:g.51950067C>G	GRCh38
NC_000013.10:g.52524203C>G , CM000675.1:g.52524203C>G	GRCh37
NC_000013.9:g.51422204C>G	NCBI36
NG_008806.1:g.66428G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*503G>C	ENSP00000489512.2:n.*503G>C
ENST00000673864.2:c.*1414G>C	ENSP00000501045.2:n.*1414G>C
ENST00000674147.2:c.2184G>C	ENSP00000500964.2:p.Val728=
ENST00000242839.10:c.2670G>C MANE Select	ENSP00000242839.5:p.Val890=
ENST00000344297.9:c.2184G>C	ENSP00000342559.5:p.Val728=
ENST00000400366.6:c.2337G>C	ENSP00000383217.3:p.Val779=
ENST00000448424.7:c.2418G>C	ENSP00000416738.3:p.Val806=
ENST00000673772.1:c.2436G>C	ENSP00000501168.1:p.Val812=
ENST00000674147.1:c.1740G>C	ENSP00000500964.1:p.Val580=
ENST00000242839.8:c.2670G>C	ENSP00000242839.4:p.Val890=
ENST00000344297.8:c.2184G>C	ENSP00000342559.5:p.Val728=
ENST00000400366.5:c.2337G>C	ENSP00000383217.3:p.Val779=
ENST00000400370.8:c.1380G>C	ENSP00000383221.3:p.Val460=
ENST00000418097.7:c.2670G>C	ENSP00000393343.2:p.Val890=
ENST00000448424.6:c.2436G>C	ENSP00000416738.2:p.Val812=
ENST00000634296.1:c.631G>C
ENST00000634308.1:c.2436G>C	ENSP00000489234.1:p.Val812=
ENST00000634620.1:n.3468G>C
ENST00000634810.1:n.2015G>C
ENST00000634844.1:c.2526G>C	ENSP00000489398.1:p.Val842=
ENST00000635406.1:n.212-3589G>C
NM_000053.3:c.2670G>C	NP_000044.2:p.Val890=
NM_001005918.2:c.2184G>C	NP_001005918.1:p.Val728=
NM_001243182.1:c.2337G>C	NP_001230111.1:p.Val779=
XM_005266423.2:c.2574G>C	XP_005266480.1:p.Val858=
XM_005266424.3:c.2574G>C	XP_005266481.1:p.Val858=
XM_005266427.2:c.2436G>C	XP_005266484.1:p.Val812=
XM_005266428.1:c.2418G>C	XP_005266485.1:p.Val806=
XM_005266430.3:c.2670G>C	XP_005266487.1:p.Val890=
XM_005266431.2:c.2634G>C	XP_005266488.1:p.Val878=
XM_005266432.2:c.2184G>C	XP_005266489.1:p.Val728=
XM_006719837.2:c.2574G>C	XP_006719900.1:p.Val858=
XM_006719838.1:c.486G>C	XP_006719901.1:p.Val162=
XM_006719839.1:c.486G>C	XP_006719902.1:p.Val162=
XM_011535117.1:c.2574G>C	XP_011533419.1:p.Val858=
XM_011535118.1:c.2670G>C	XP_011533420.1:p.Val890=
XM_011535119.1:c.2670G>C	XP_011533421.1:p.Val890=
XM_011535120.1:c.2256G>C	XP_011533422.1:p.Val752=
XM_011535121.1:c.2670G>C	XP_011533423.1:p.Val890=
XM_011535122.1:c.1338G>C	XP_011533424.1:p.Val446=
XR_941601.1:n.2889G>C
XR_941602.1:n.2889G>C
XR_941603.1:n.2889G>C
XR_941604.1:n.2889G>C
NM_001330578.1:c.2436G>C	NP_001317507.1:p.Val812=
NM_001330579.1:c.2418G>C	NP_001317508.1:p.Val806=
XM_005266424.4:c.2574G>C	XP_005266481.1:p.Val858=
XM_005266430.4:c.2670G>C	XP_005266487.1:p.Val890=
XM_005266431.4:c.2634G>C	XP_005266488.1:p.Val878=
XM_006719837.3:c.2574G>C	XP_006719900.1:p.Val858=
XM_011535117.3:c.2574G>C	XP_011533419.1:p.Val858=
XM_017020627.1:c.2574G>C	XP_016876116.1:p.Val858=
NM_000053.4:c.2670G>C MANE Select	NP_000044.2:p.Val890=
NM_001005918.3:c.2184G>C	NP_001005918.1:p.Val728=
NM_001330579.2:c.2418G>C	NP_001317508.1:p.Val806=
NM_001243182.2:c.2337G>C	NP_001230111.1:p.Val779=
NM_001330578.2:c.2436G>C	NP_001317507.1:p.Val812=