Canonical Allele Identifier: CA388026557

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515313G>C (hg19) ; chr13:g.51941177G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941177G>C , CM000675.2:g.51941177G>C	GRCh38
NC_000013.10:g.52515313G>C , CM000675.1:g.52515313G>C	GRCh37
NC_000013.9:g.51413314G>C	NCBI36
NG_008806.1:g.75318C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1110C>G	ENSP00000489512.2:n.*1110C>G
ENST00000673864.2:c.*2204C>G	ENSP00000501045.2:n.*2204C>G
ENST00000674147.2:c.2839C>G	ENSP00000500964.2:p.Leu947Val
ENST00000242839.10:c.3460C>G MANE Select	ENSP00000242839.5:p.Leu1154Val
ENST00000344297.9:c.2839C>G	ENSP00000342559.5:p.Leu947Val
ENST00000400366.6:c.3127C>G	ENSP00000383217.3:p.Leu1043Val
ENST00000448424.7:c.3208C>G	ENSP00000416738.3:p.Leu1070Val
ENST00000673772.1:c.3226C>G	ENSP00000501168.1:p.Leu1076Val
ENST00000673867.1:n.3599C>G
ENST00000674126.1:n.3823C>G
ENST00000674147.1:c.2395C>G	ENSP00000500964.1:p.Leu799Val
ENST00000242839.8:c.3460C>G	ENSP00000242839.4:p.Leu1154Val
ENST00000344297.8:c.2839C>G	ENSP00000342559.5:p.Leu947Val
ENST00000400366.5:c.3127C>G	ENSP00000383217.3:p.Leu1043Val
ENST00000400370.8:c.2170C>G	ENSP00000383221.3:p.Leu724Val
ENST00000418097.7:c.3265C>G	ENSP00000393343.2:p.Leu1089Val
ENST00000448424.6:c.3226C>G	ENSP00000416738.2:p.Leu1076Val
ENST00000634296.1:c.1238C>G
ENST00000634308.1:c.*561C>G	ENSP00000489234.1:n.*561C>G
ENST00000634620.1:n.4204C>G
ENST00000634810.1:n.2805C>G
ENST00000634844.1:c.3316C>G	ENSP00000489398.1:p.Leu1106Val
NM_000053.3:c.3460C>G	NP_000044.2:p.Leu1154Val
NM_001005918.2:c.2839C>G	NP_001005918.1:p.Leu947Val
NM_001243182.1:c.3127C>G	NP_001230111.1:p.Leu1043Val
XM_005266423.2:c.3364C>G	XP_005266480.1:p.Leu1122Val
XM_005266424.3:c.3364C>G	XP_005266481.1:p.Leu1122Val
XM_005266427.2:c.3226C>G	XP_005266484.1:p.Leu1076Val
XM_005266428.1:c.3208C>G	XP_005266485.1:p.Leu1070Val
XM_005266430.3:c.3460C>G	XP_005266487.1:p.Leu1154Val
XM_005266431.2:c.3424C>G	XP_005266488.1:p.Leu1142Val
XM_005266432.2:c.2974C>G	XP_005266489.1:p.Leu992Val
XM_006719837.2:c.3364C>G	XP_006719900.1:p.Leu1122Val
XM_006719838.1:c.1276C>G	XP_006719901.1:p.Leu426Val
XM_006719839.1:c.1093C>G	XP_006719902.1:p.Leu365Val
XM_011535117.1:c.3364C>G	XP_011533419.1:p.Leu1122Val
XM_011535118.1:c.3325C>G	XP_011533420.1:p.Leu1109Val
XM_011535119.1:c.3277C>G	XP_011533421.1:p.Leu1093Val
XM_011535120.1:c.3046C>G	XP_011533422.1:p.Leu1016Val
XM_011535121.1:c.2947C>G	XP_011533423.1:p.Leu983Val
XM_011535122.1:c.2128C>G	XP_011533424.1:p.Leu710Val
XR_941601.1:n.3679C>G
XR_941602.1:n.3679C>G
XR_941603.1:n.3679C>G
XR_941604.1:n.3679C>G
NM_001330578.1:c.3226C>G	NP_001317507.1:p.Leu1076Val
NM_001330579.1:c.3208C>G	NP_001317508.1:p.Leu1070Val
XM_005266424.4:c.3364C>G	XP_005266481.1:p.Leu1122Val
XM_005266430.4:c.3460C>G	XP_005266487.1:p.Leu1154Val
XM_005266431.4:c.3424C>G	XP_005266488.1:p.Leu1142Val
XM_006719837.3:c.3364C>G	XP_006719900.1:p.Leu1122Val
XM_011535117.3:c.3364C>G	XP_011533419.1:p.Leu1122Val
XM_017020627.1:c.3364C>G	XP_016876116.1:p.Leu1122Val
NM_000053.4:c.3460C>G MANE Select	NP_000044.2:p.Leu1154Val
NM_001005918.3:c.2839C>G	NP_001005918.1:p.Leu947Val
NM_001330579.2:c.3208C>G	NP_001317508.1:p.Leu1070Val
NM_001243182.2:c.3127C>G	NP_001230111.1:p.Leu1043Val
NM_001330578.2:c.3226C>G	NP_001317507.1:p.Leu1076Val