Canonical Allele Identifier: CA388020477

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52532464G>T (hg19) ; chr13:g.51958328G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51958328G>T , CM000675.2:g.51958328G>T	GRCh38
NC_000013.10:g.52532464G>T , CM000675.1:g.52532464G>T	GRCh37
NC_000013.9:g.51430465G>T	NCBI36
NG_008806.1:g.58167C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*171C>A	ENSP00000489512.2:n.*171C>A
ENST00000673864.2:c.*1082C>A	ENSP00000501045.2:n.*1082C>A
ENST00000674147.2:c.1870-721C>A	ENSP00000500964.2:n.1870-721C>A
ENST00000242839.10:c.2338C>A MANE Select	ENSP00000242839.5:p.Leu780Met
ENST00000344297.9:c.1870-721C>A	ENSP00000342559.5:n.1870-721C>A
ENST00000400366.6:c.2005C>A	ENSP00000383217.3:p.Leu669Met
ENST00000448424.7:c.2086C>A	ENSP00000416738.3:p.Leu696Met
ENST00000673772.1:c.2122-721C>A	ENSP00000501168.1:n.2122-721C>A
ENST00000674147.1:c.1426-721C>A	ENSP00000500964.1:n.1426-721C>A
ENST00000242839.8:c.2338C>A	ENSP00000242839.4:p.Leu780Met
ENST00000344297.8:c.1870-721C>A	ENSP00000342559.5:n.1870-721C>A
ENST00000400366.5:c.2005C>A	ENSP00000383217.3:p.Leu669Met
ENST00000400370.8:c.1286-8167C>A	ENSP00000383221.3:n.1286-8167C>A
ENST00000418097.7:c.2338C>A	ENSP00000393343.2:p.Leu780Met
ENST00000448424.6:c.2122-721C>A	ENSP00000416738.2:n.2122-721C>A
ENST00000634296.1:c.299C>A
ENST00000634308.1:c.2122-721C>A	ENSP00000489234.1:n.2122-721C>A
ENST00000634620.1:n.2433C>A
ENST00000634810.1:n.1683C>A
ENST00000634844.1:c.2194C>A	ENSP00000489398.1:p.Leu732Met
ENST00000635406.1:n.212-11850C>A
NM_000053.3:c.2338C>A	NP_000044.2:p.Leu780Met
NM_001005918.2:c.1870-721C>A	NP_001005918.1:n.1870-721C>A
NM_001243182.1:c.2005C>A	NP_001230111.1:p.Leu669Met
XM_005266423.2:c.2242C>A	XP_005266480.1:p.Leu748Met
XM_005266424.3:c.2242C>A	XP_005266481.1:p.Leu748Met
XM_005266427.2:c.2122-721C>A	XP_005266484.1:n.2122-721C>A
XM_005266428.1:c.2086C>A	XP_005266485.1:p.Leu696Met
XM_005266430.3:c.2338C>A	XP_005266487.1:p.Leu780Met
XM_005266431.2:c.2302C>A	XP_005266488.1:p.Leu768Met
XM_005266432.2:c.1870-721C>A	XP_005266489.1:n.1870-721C>A
XM_006719837.2:c.2242C>A	XP_006719900.1:p.Leu748Met
XM_006719838.1:c.154C>A	XP_006719901.1:p.Leu52Met
XM_006719839.1:c.154C>A	XP_006719902.1:p.Leu52Met
XM_011535117.1:c.2242C>A	XP_011533419.1:p.Leu748Met
XM_011535118.1:c.2338C>A	XP_011533420.1:p.Leu780Met
XM_011535119.1:c.2338C>A	XP_011533421.1:p.Leu780Met
XM_011535120.1:c.1924C>A	XP_011533422.1:p.Leu642Met
XM_011535121.1:c.2338C>A	XP_011533423.1:p.Leu780Met
XM_011535122.1:c.1006C>A	XP_011533424.1:p.Leu336Met
XR_941601.1:n.2557C>A
XR_941602.1:n.2557C>A
XR_941603.1:n.2557C>A
XR_941604.1:n.2557C>A
NM_001330578.1:c.2122-721C>A	NP_001317507.1:n.2122-721C>A
NM_001330579.1:c.2086C>A	NP_001317508.1:p.Leu696Met
XM_005266424.4:c.2242C>A	XP_005266481.1:p.Leu748Met
XM_005266430.4:c.2338C>A	XP_005266487.1:p.Leu780Met
XM_005266431.4:c.2302C>A	XP_005266488.1:p.Leu768Met
XM_006719837.3:c.2242C>A	XP_006719900.1:p.Leu748Met
XM_011535117.3:c.2242C>A	XP_011533419.1:p.Leu748Met
XM_017020627.1:c.2242C>A	XP_016876116.1:p.Leu748Met
NM_000053.4:c.2338C>A MANE Select	NP_000044.2:p.Leu780Met
NM_001005918.3:c.1870-721C>A	NP_001005918.1:n.1870-721C>A
NM_001330579.2:c.2086C>A	NP_001317508.1:p.Leu696Met
NM_001243182.2:c.2005C>A	NP_001230111.1:p.Leu669Met
NM_001330578.2:c.2122-721C>A	NP_001317507.1:n.2122-721C>A