Canonical Allele Identifier: CA483894741

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52518377G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944241G>A , CM000675.2:g.51944241G>A	GRCh38
NC_000013.10:g.52518377G>A , CM000675.1:g.52518377G>A	GRCh37
NC_000013.9:g.51416378G>A	NCBI36
NG_008806.1:g.72254C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*894-1687C>T	ENSP00000489512.2:n.*894-1687C>T
ENST00000673864.2:c.*1855C>T	ENSP00000501045.2:n.*1855C>T
ENST00000674147.2:c.2490C>T	ENSP00000500964.2:p.Pro830=
ENST00000242839.10:c.3111C>T MANE Select	ENSP00000242839.5:p.Pro1037=
ENST00000344297.9:c.2490C>T	ENSP00000342559.5:p.Pro830=
ENST00000400366.6:c.2778C>T	ENSP00000383217.3:p.Pro926=
ENST00000448424.7:c.2859C>T	ENSP00000416738.3:p.Pro953=
ENST00000673772.1:c.2877C>T	ENSP00000501168.1:p.Pro959=
ENST00000673867.1:n.3250C>T
ENST00000674126.1:n.3474C>T
ENST00000674147.1:c.2046C>T	ENSP00000500964.1:p.Pro682=
ENST00000242839.8:c.3111C>T	ENSP00000242839.4:p.Pro1037=
ENST00000344297.8:c.2490C>T	ENSP00000342559.5:p.Pro830=
ENST00000400366.5:c.2778C>T	ENSP00000383217.3:p.Pro926=
ENST00000400370.8:c.1821C>T	ENSP00000383221.3:p.Pro607=
ENST00000418097.7:c.2916C>T	ENSP00000393343.2:p.Pro972=
ENST00000448424.6:c.2877C>T	ENSP00000416738.2:p.Pro959=
ENST00000466629.1:n.331C>T
ENST00000634296.1:c.1022-1687C>T
ENST00000634308.1:c.*212C>T	ENSP00000489234.1:n.*212C>T
ENST00000634620.1:n.3855C>T
ENST00000634810.1:n.2456C>T
ENST00000634844.1:c.2967C>T	ENSP00000489398.1:p.Pro989=
ENST00000635406.1:n.457C>T
NM_000053.3:c.3111C>T	NP_000044.2:p.Pro1037=
NM_001005918.2:c.2490C>T	NP_001005918.1:p.Pro830=
NM_001243182.1:c.2778C>T	NP_001230111.1:p.Pro926=
XM_005266423.2:c.3015C>T	XP_005266480.1:p.Pro1005=
XM_005266424.3:c.3015C>T	XP_005266481.1:p.Pro1005=
XM_005266427.2:c.2877C>T	XP_005266484.1:p.Pro959=
XM_005266428.1:c.2859C>T	XP_005266485.1:p.Pro953=
XM_005266430.3:c.3111C>T	XP_005266487.1:p.Pro1037=
XM_005266431.2:c.3075C>T	XP_005266488.1:p.Pro1025=
XM_005266432.2:c.2625C>T	XP_005266489.1:p.Pro875=
XM_006719837.2:c.3015C>T	XP_006719900.1:p.Pro1005=
XM_006719838.1:c.927C>T	XP_006719901.1:p.Pro309=
XM_006719839.1:c.877-1687C>T	XP_006719902.1:n.877-1687C>T
XM_011535117.1:c.3015C>T	XP_011533419.1:p.Pro1005=
XM_011535118.1:c.2976C>T	XP_011533420.1:p.Pro992=
XM_011535119.1:c.3061-1687C>T	XP_011533421.1:n.3061-1687C>T
XM_011535120.1:c.2697C>T	XP_011533422.1:p.Pro899=
XM_011535121.1:c.2731-1687C>T	XP_011533423.1:n.2731-1687C>T
XM_011535122.1:c.1779C>T	XP_011533424.1:p.Pro593=
XR_941601.1:n.3330C>T
XR_941602.1:n.3330C>T
XR_941603.1:n.3330C>T
XR_941604.1:n.3330C>T
NM_001330578.1:c.2877C>T	NP_001317507.1:p.Pro959=
NM_001330579.1:c.2859C>T	NP_001317508.1:p.Pro953=
XM_005266424.4:c.3015C>T	XP_005266481.1:p.Pro1005=
XM_005266430.4:c.3111C>T	XP_005266487.1:p.Pro1037=
XM_005266431.4:c.3075C>T	XP_005266488.1:p.Pro1025=
XM_006719837.3:c.3015C>T	XP_006719900.1:p.Pro1005=
XM_011535117.3:c.3015C>T	XP_011533419.1:p.Pro1005=
XM_017020627.1:c.3015C>T	XP_016876116.1:p.Pro1005=
NM_000053.4:c.3111C>T MANE Select	NP_000044.2:p.Pro1037=
NM_001005918.3:c.2490C>T	NP_001005918.1:p.Pro830=
NM_001330579.2:c.2859C>T	NP_001317508.1:p.Pro953=
NM_001243182.2:c.2778C>T	NP_001230111.1:p.Pro926=
NM_001330578.2:c.2877C>T	NP_001317507.1:p.Pro959=