Canonical Allele Identifier: CA171311

Gene: ATP7B

Linked Data

• ClinVar Variation Id: 157946
• ClinVar RCV Id: RCV000145271
• dbSNP Id: rs587783310
• MyVariant Identifiers: chr13:g.52518278G>A (hg19) ; chr13:g.51944142G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944142G>A , CM000675.2:g.51944142G>A	GRCh38
NC_000013.10:g.52518278G>A , CM000675.1:g.52518278G>A	GRCh37
NC_000013.9:g.51416279G>A	NCBI36
NG_008806.1:g.72353C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*894-1588C>T	ENSP00000489512.2:n.*894-1588C>T
ENST00000673864.2:c.*1954C>T	ENSP00000501045.2:n.*1954C>T
ENST00000674147.2:c.2589C>T	ENSP00000500964.2:p.Pro863=
ENST00000242839.10:c.3210C>T MANE Select	ENSP00000242839.5:p.Pro1070=
ENST00000344297.9:c.2589C>T	ENSP00000342559.5:p.Pro863=
ENST00000400366.6:c.2877C>T	ENSP00000383217.3:p.Pro959=
ENST00000448424.7:c.2958C>T	ENSP00000416738.3:p.Pro986=
ENST00000673772.1:c.2976C>T	ENSP00000501168.1:p.Pro992=
ENST00000673867.1:n.3349C>T
ENST00000674126.1:n.3573C>T
ENST00000674147.1:c.2145C>T	ENSP00000500964.1:p.Pro715=
ENST00000242839.8:c.3210C>T	ENSP00000242839.4:p.Pro1070=
ENST00000344297.8:c.2589C>T	ENSP00000342559.5:p.Pro863=
ENST00000400366.5:c.2877C>T	ENSP00000383217.3:p.Pro959=
ENST00000400370.8:c.1920C>T	ENSP00000383221.3:p.Pro640=
ENST00000418097.7:c.3015C>T	ENSP00000393343.2:p.Pro1005=
ENST00000448424.6:c.2976C>T	ENSP00000416738.2:p.Pro992=
ENST00000466629.1:n.430C>T
ENST00000634296.1:c.1022-1588C>T
ENST00000634308.1:c.*311C>T	ENSP00000489234.1:n.*311C>T
ENST00000634620.1:n.3954C>T
ENST00000634810.1:n.2555C>T
ENST00000634844.1:c.3066C>T	ENSP00000489398.1:p.Pro1022=
NM_000053.3:c.3210C>T	NP_000044.2:p.Pro1070=
NM_001005918.2:c.2589C>T	NP_001005918.1:p.Pro863=
NM_001243182.1:c.2877C>T	NP_001230111.1:p.Pro959=
XM_005266423.2:c.3114C>T	XP_005266480.1:p.Pro1038=
XM_005266424.3:c.3114C>T	XP_005266481.1:p.Pro1038=
XM_005266427.2:c.2976C>T	XP_005266484.1:p.Pro992=
XM_005266428.1:c.2958C>T	XP_005266485.1:p.Pro986=
XM_005266430.3:c.3210C>T	XP_005266487.1:p.Pro1070=
XM_005266431.2:c.3174C>T	XP_005266488.1:p.Pro1058=
XM_005266432.2:c.2724C>T	XP_005266489.1:p.Pro908=
XM_006719837.2:c.3114C>T	XP_006719900.1:p.Pro1038=
XM_006719838.1:c.1026C>T	XP_006719901.1:p.Pro342=
XM_006719839.1:c.877-1588C>T	XP_006719902.1:n.877-1588C>T
XM_011535117.1:c.3114C>T	XP_011533419.1:p.Pro1038=
XM_011535118.1:c.3075C>T	XP_011533420.1:p.Pro1025=
XM_011535119.1:c.3061-1588C>T	XP_011533421.1:n.3061-1588C>T
XM_011535120.1:c.2796C>T	XP_011533422.1:p.Pro932=
XM_011535121.1:c.2731-1588C>T	XP_011533423.1:n.2731-1588C>T
XM_011535122.1:c.1878C>T	XP_011533424.1:p.Pro626=
XR_941601.1:n.3429C>T
XR_941602.1:n.3429C>T
XR_941603.1:n.3429C>T
XR_941604.1:n.3429C>T
NM_001330578.1:c.2976C>T	NP_001317507.1:p.Pro992=
NM_001330579.1:c.2958C>T	NP_001317508.1:p.Pro986=
XM_005266424.4:c.3114C>T	XP_005266481.1:p.Pro1038=
XM_005266430.4:c.3210C>T	XP_005266487.1:p.Pro1070=
XM_005266431.4:c.3174C>T	XP_005266488.1:p.Pro1058=
XM_006719837.3:c.3114C>T	XP_006719900.1:p.Pro1038=
XM_011535117.3:c.3114C>T	XP_011533419.1:p.Pro1038=
XM_017020627.1:c.3114C>T	XP_016876116.1:p.Pro1038=
NM_000053.4:c.3210C>T MANE Select	NP_000044.2:p.Pro1070=
NM_001005918.3:c.2589C>T	NP_001005918.1:p.Pro863=
NM_001330579.2:c.2958C>T	NP_001317508.1:p.Pro986=
NM_001243182.2:c.2877C>T	NP_001230111.1:p.Pro959=
NM_001330578.2:c.2976C>T	NP_001317507.1:p.Pro992=