Canonical Allele Identifier: CA388029795

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52518257T>G (hg19) ; chr13:g.51944121T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944121T>G , CM000675.2:g.51944121T>G	GRCh38
NC_000013.10:g.52518257T>G , CM000675.1:g.52518257T>G	GRCh37
NC_000013.9:g.51416258T>G	NCBI36
NG_008806.1:g.72374A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1567A>C	ENSP00000489512.2:n.*894-1567A>C
ENST00000673864.2:c.*1975A>C	ENSP00000501045.2:n.*1975A>C
ENST00000674147.2:c.2610A>C	ENSP00000500964.2:p.Lys870Asn
ENST00000242839.10:c.3231A>C MANE Select	ENSP00000242839.5:p.Lys1077Asn
ENST00000344297.9:c.2610A>C	ENSP00000342559.5:p.Lys870Asn
ENST00000400366.6:c.2898A>C	ENSP00000383217.3:p.Lys966Asn
ENST00000448424.7:c.2979A>C	ENSP00000416738.3:p.Lys993Asn
ENST00000673772.1:c.2997A>C	ENSP00000501168.1:p.Lys999Asn
ENST00000673867.1:n.3370A>C
ENST00000674126.1:n.3594A>C
ENST00000674147.1:c.2166A>C	ENSP00000500964.1:p.Lys722Asn
ENST00000242839.8:c.3231A>C	ENSP00000242839.4:p.Lys1077Asn
ENST00000344297.8:c.2610A>C	ENSP00000342559.5:p.Lys870Asn
ENST00000400366.5:c.2898A>C	ENSP00000383217.3:p.Lys966Asn
ENST00000400370.8:c.1941A>C	ENSP00000383221.3:p.Lys647Asn
ENST00000418097.7:c.3036A>C	ENSP00000393343.2:p.Lys1012Asn
ENST00000448424.6:c.2997A>C	ENSP00000416738.2:p.Lys999Asn
ENST00000466629.1:n.451A>C
ENST00000634296.1:c.1022-1567A>C
ENST00000634308.1:c.*332A>C	ENSP00000489234.1:n.*332A>C
ENST00000634620.1:n.3975A>C
ENST00000634810.1:n.2576A>C
ENST00000634844.1:c.3087A>C	ENSP00000489398.1:p.Lys1029Asn
NM_000053.3:c.3231A>C	NP_000044.2:p.Lys1077Asn
NM_001005918.2:c.2610A>C	NP_001005918.1:p.Lys870Asn
NM_001243182.1:c.2898A>C	NP_001230111.1:p.Lys966Asn
XM_005266423.2:c.3135A>C	XP_005266480.1:p.Lys1045Asn
XM_005266424.3:c.3135A>C	XP_005266481.1:p.Lys1045Asn
XM_005266427.2:c.2997A>C	XP_005266484.1:p.Lys999Asn
XM_005266428.1:c.2979A>C	XP_005266485.1:p.Lys993Asn
XM_005266430.3:c.3231A>C	XP_005266487.1:p.Lys1077Asn
XM_005266431.2:c.3195A>C	XP_005266488.1:p.Lys1065Asn
XM_005266432.2:c.2745A>C	XP_005266489.1:p.Lys915Asn
XM_006719837.2:c.3135A>C	XP_006719900.1:p.Lys1045Asn
XM_006719838.1:c.1047A>C	XP_006719901.1:p.Lys349Asn
XM_006719839.1:c.877-1567A>C	XP_006719902.1:n.877-1567A>C
XM_011535117.1:c.3135A>C	XP_011533419.1:p.Lys1045Asn
XM_011535118.1:c.3096A>C	XP_011533420.1:p.Lys1032Asn
XM_011535119.1:c.3061-1567A>C	XP_011533421.1:n.3061-1567A>C
XM_011535120.1:c.2817A>C	XP_011533422.1:p.Lys939Asn
XM_011535121.1:c.2731-1567A>C	XP_011533423.1:n.2731-1567A>C
XM_011535122.1:c.1899A>C	XP_011533424.1:p.Lys633Asn
XR_941601.1:n.3450A>C
XR_941602.1:n.3450A>C
XR_941603.1:n.3450A>C
XR_941604.1:n.3450A>C
NM_001330578.1:c.2997A>C	NP_001317507.1:p.Lys999Asn
NM_001330579.1:c.2979A>C	NP_001317508.1:p.Lys993Asn
XM_005266424.4:c.3135A>C	XP_005266481.1:p.Lys1045Asn
XM_005266430.4:c.3231A>C	XP_005266487.1:p.Lys1077Asn
XM_005266431.4:c.3195A>C	XP_005266488.1:p.Lys1065Asn
XM_006719837.3:c.3135A>C	XP_006719900.1:p.Lys1045Asn
XM_011535117.3:c.3135A>C	XP_011533419.1:p.Lys1045Asn
XM_017020627.1:c.3135A>C	XP_016876116.1:p.Lys1045Asn
NM_000053.4:c.3231A>C MANE Select	NP_000044.2:p.Lys1077Asn
NM_001005918.3:c.2610A>C	NP_001005918.1:p.Lys870Asn
NM_001330579.2:c.2979A>C	NP_001317508.1:p.Lys993Asn
NM_001243182.2:c.2898A>C	NP_001230111.1:p.Lys966Asn
NM_001330578.2:c.2997A>C	NP_001317507.1:p.Lys999Asn