Canonical Allele Identifier: CA388034296

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52524185C>G (hg19) ; chr13:g.51950049C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51950049C>G , CM000675.2:g.51950049C>G	GRCh38
NC_000013.10:g.52524185C>G , CM000675.1:g.52524185C>G	GRCh37
NC_000013.9:g.51422186C>G	NCBI36
NG_008806.1:g.66446G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*521G>C	ENSP00000489512.2:n.*521G>C
ENST00000673864.2:c.*1432G>C	ENSP00000501045.2:n.*1432G>C
ENST00000674147.2:c.2202G>C	ENSP00000500964.2:p.Leu734Phe
ENST00000242839.10:c.2688G>C MANE Select	ENSP00000242839.5:p.Leu896Phe
ENST00000344297.9:c.2202G>C	ENSP00000342559.5:p.Leu734Phe
ENST00000400366.6:c.2355G>C	ENSP00000383217.3:p.Leu785Phe
ENST00000448424.7:c.2436G>C	ENSP00000416738.3:p.Leu812Phe
ENST00000673772.1:c.2454G>C	ENSP00000501168.1:p.Leu818Phe
ENST00000674147.1:c.1758G>C	ENSP00000500964.1:p.Leu586Phe
ENST00000242839.8:c.2688G>C	ENSP00000242839.4:p.Leu896Phe
ENST00000344297.8:c.2202G>C	ENSP00000342559.5:p.Leu734Phe
ENST00000400366.5:c.2355G>C	ENSP00000383217.3:p.Leu785Phe
ENST00000400370.8:c.1398G>C	ENSP00000383221.3:p.Leu466Phe
ENST00000418097.7:c.2688G>C	ENSP00000393343.2:p.Leu896Phe
ENST00000448424.6:c.2454G>C	ENSP00000416738.2:p.Leu818Phe
ENST00000634296.1:c.649G>C
ENST00000634308.1:c.2454G>C	ENSP00000489234.1:p.Leu818Phe
ENST00000634620.1:n.3486G>C
ENST00000634810.1:n.2033G>C
ENST00000634844.1:c.2544G>C	ENSP00000489398.1:p.Leu848Phe
ENST00000635406.1:n.212-3571G>C
NM_000053.3:c.2688G>C	NP_000044.2:p.Leu896Phe
NM_001005918.2:c.2202G>C	NP_001005918.1:p.Leu734Phe
NM_001243182.1:c.2355G>C	NP_001230111.1:p.Leu785Phe
XM_005266423.2:c.2592G>C	XP_005266480.1:p.Leu864Phe
XM_005266424.3:c.2592G>C	XP_005266481.1:p.Leu864Phe
XM_005266427.2:c.2454G>C	XP_005266484.1:p.Leu818Phe
XM_005266428.1:c.2436G>C	XP_005266485.1:p.Leu812Phe
XM_005266430.3:c.2688G>C	XP_005266487.1:p.Leu896Phe
XM_005266431.2:c.2652G>C	XP_005266488.1:p.Leu884Phe
XM_005266432.2:c.2202G>C	XP_005266489.1:p.Leu734Phe
XM_006719837.2:c.2592G>C	XP_006719900.1:p.Leu864Phe
XM_006719838.1:c.504G>C	XP_006719901.1:p.Leu168Phe
XM_006719839.1:c.504G>C	XP_006719902.1:p.Leu168Phe
XM_011535117.1:c.2592G>C	XP_011533419.1:p.Leu864Phe
XM_011535118.1:c.2688G>C	XP_011533420.1:p.Leu896Phe
XM_011535119.1:c.2688G>C	XP_011533421.1:p.Leu896Phe
XM_011535120.1:c.2274G>C	XP_011533422.1:p.Leu758Phe
XM_011535121.1:c.2688G>C	XP_011533423.1:p.Leu896Phe
XM_011535122.1:c.1356G>C	XP_011533424.1:p.Leu452Phe
XR_941601.1:n.2907G>C
XR_941602.1:n.2907G>C
XR_941603.1:n.2907G>C
XR_941604.1:n.2907G>C
NM_001330578.1:c.2454G>C	NP_001317507.1:p.Leu818Phe
NM_001330579.1:c.2436G>C	NP_001317508.1:p.Leu812Phe
XM_005266424.4:c.2592G>C	XP_005266481.1:p.Leu864Phe
XM_005266430.4:c.2688G>C	XP_005266487.1:p.Leu896Phe
XM_005266431.4:c.2652G>C	XP_005266488.1:p.Leu884Phe
XM_006719837.3:c.2592G>C	XP_006719900.1:p.Leu864Phe
XM_011535117.3:c.2592G>C	XP_011533419.1:p.Leu864Phe
XM_017020627.1:c.2592G>C	XP_016876116.1:p.Leu864Phe
NM_000053.4:c.2688G>C MANE Select	NP_000044.2:p.Leu896Phe
NM_001005918.3:c.2202G>C	NP_001005918.1:p.Leu734Phe
NM_001330579.2:c.2436G>C	NP_001317508.1:p.Leu812Phe
NM_001243182.2:c.2355G>C	NP_001230111.1:p.Leu785Phe
NM_001330578.2:c.2454G>C	NP_001317507.1:p.Leu818Phe