Canonical Allele Identifier: CA388028878

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52516670C>A (hg19) ; chr13:g.51942534C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51942534C>A , CM000675.2:g.51942534C>A	GRCh38
NC_000013.10:g.52516670C>A , CM000675.1:g.52516670C>A	GRCh37
NC_000013.9:g.51414671C>A	NCBI36
NG_008806.1:g.73961G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*914G>T	ENSP00000489512.2:n.*914G>T
ENST00000673864.2:c.*2008G>T	ENSP00000501045.2:n.*2008G>T
ENST00000674147.2:c.2643G>T	ENSP00000500964.2:p.Leu881Phe
ENST00000242839.10:c.3264G>T MANE Select	ENSP00000242839.5:p.Leu1088Phe
ENST00000344297.9:c.2643G>T	ENSP00000342559.5:p.Leu881Phe
ENST00000400366.6:c.2931G>T	ENSP00000383217.3:p.Leu977Phe
ENST00000448424.7:c.3012G>T	ENSP00000416738.3:p.Leu1004Phe
ENST00000673772.1:c.3030G>T	ENSP00000501168.1:p.Leu1010Phe
ENST00000673867.1:n.3403G>T
ENST00000674126.1:n.3627G>T
ENST00000674147.1:c.2199G>T	ENSP00000500964.1:p.Leu733Phe
ENST00000242839.8:c.3264G>T	ENSP00000242839.4:p.Leu1088Phe
ENST00000344297.8:c.2643G>T	ENSP00000342559.5:p.Leu881Phe
ENST00000400366.5:c.2931G>T	ENSP00000383217.3:p.Leu977Phe
ENST00000400370.8:c.1974G>T	ENSP00000383221.3:p.Leu658Phe
ENST00000418097.7:c.3069G>T	ENSP00000393343.2:p.Leu1023Phe
ENST00000448424.6:c.3030G>T	ENSP00000416738.2:p.Leu1010Phe
ENST00000634296.1:c.1042G>T
ENST00000634308.1:c.*365G>T	ENSP00000489234.1:n.*365G>T
ENST00000634620.1:n.4008G>T
ENST00000634810.1:n.2609G>T
ENST00000634844.1:c.3120G>T	ENSP00000489398.1:p.Leu1040Phe
NM_000053.3:c.3264G>T	NP_000044.2:p.Leu1088Phe
NM_001005918.2:c.2643G>T	NP_001005918.1:p.Leu881Phe
NM_001243182.1:c.2931G>T	NP_001230111.1:p.Leu977Phe
XM_005266423.2:c.3168G>T	XP_005266480.1:p.Leu1056Phe
XM_005266424.3:c.3168G>T	XP_005266481.1:p.Leu1056Phe
XM_005266427.2:c.3030G>T	XP_005266484.1:p.Leu1010Phe
XM_005266428.1:c.3012G>T	XP_005266485.1:p.Leu1004Phe
XM_005266430.3:c.3264G>T	XP_005266487.1:p.Leu1088Phe
XM_005266431.2:c.3228G>T	XP_005266488.1:p.Leu1076Phe
XM_005266432.2:c.2778G>T	XP_005266489.1:p.Leu926Phe
XM_006719837.2:c.3168G>T	XP_006719900.1:p.Leu1056Phe
XM_006719838.1:c.1080G>T	XP_006719901.1:p.Leu360Phe
XM_006719839.1:c.897G>T	XP_006719902.1:p.Leu299Phe
XM_011535117.1:c.3168G>T	XP_011533419.1:p.Leu1056Phe
XM_011535118.1:c.3129G>T	XP_011533420.1:p.Leu1043Phe
XM_011535119.1:c.3081G>T	XP_011533421.1:p.Leu1027Phe
XM_011535120.1:c.2850G>T	XP_011533422.1:p.Leu950Phe
XM_011535121.1:c.2751G>T	XP_011533423.1:p.Leu917Phe
XM_011535122.1:c.1932G>T	XP_011533424.1:p.Leu644Phe
XR_941601.1:n.3483G>T
XR_941602.1:n.3483G>T
XR_941603.1:n.3483G>T
XR_941604.1:n.3483G>T
NM_001330578.1:c.3030G>T	NP_001317507.1:p.Leu1010Phe
NM_001330579.1:c.3012G>T	NP_001317508.1:p.Leu1004Phe
XM_005266424.4:c.3168G>T	XP_005266481.1:p.Leu1056Phe
XM_005266430.4:c.3264G>T	XP_005266487.1:p.Leu1088Phe
XM_005266431.4:c.3228G>T	XP_005266488.1:p.Leu1076Phe
XM_006719837.3:c.3168G>T	XP_006719900.1:p.Leu1056Phe
XM_011535117.3:c.3168G>T	XP_011533419.1:p.Leu1056Phe
XM_017020627.1:c.3168G>T	XP_016876116.1:p.Leu1056Phe
NM_000053.4:c.3264G>T MANE Select	NP_000044.2:p.Leu1088Phe
NM_001005918.3:c.2643G>T	NP_001005918.1:p.Leu881Phe
NM_001330579.2:c.3012G>T	NP_001317508.1:p.Leu1004Phe
NM_001243182.2:c.2931G>T	NP_001230111.1:p.Leu977Phe
NM_001330578.2:c.3030G>T	NP_001317507.1:p.Leu1010Phe