Canonical Allele Identifier: CA388020264

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52509819G>A (hg19) ; chr13:g.51935683G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51935683G>A , CM000675.2:g.51935683G>A	GRCh38
NC_000013.10:g.52509819G>A , CM000675.1:g.52509819G>A	GRCh37
NC_000013.9:g.51407820G>A	NCBI36
NG_008806.1:g.80812C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1684C>T	ENSP00000489512.2:n.*1684C>T
ENST00000673864.2:c.*2778C>T	ENSP00000501045.2:n.*2778C>T
ENST00000674147.2:c.3413C>T	ENSP00000500964.2:p.Pro1138Leu
ENST00000242839.10:c.4034C>T MANE Select	ENSP00000242839.5:p.Pro1345Leu
ENST00000344297.9:c.3413C>T	ENSP00000342559.5:p.Pro1138Leu
ENST00000400366.6:c.3701C>T	ENSP00000383217.3:p.Pro1234Leu
ENST00000448424.7:c.3782C>T	ENSP00000416738.3:p.Pro1261Leu
ENST00000673696.1:n.1357C>T
ENST00000673772.1:c.3800C>T	ENSP00000501168.1:p.Pro1267Leu
ENST00000673867.1:n.4173C>T
ENST00000673923.1:n.900C>T
ENST00000674147.1:c.2969C>T	ENSP00000500964.1:p.Pro990Leu
ENST00000242839.8:c.4034C>T	ENSP00000242839.4:p.Pro1345Leu
ENST00000344297.8:c.3413C>T	ENSP00000342559.5:p.Pro1138Leu
ENST00000400366.5:c.3701C>T	ENSP00000383217.3:p.Pro1234Leu
ENST00000400370.8:c.2744C>T	ENSP00000383221.3:p.Pro915Leu
ENST00000418097.7:c.3839C>T	ENSP00000393343.2:p.Pro1280Leu
ENST00000448424.6:c.3800C>T	ENSP00000416738.2:p.Pro1267Leu
ENST00000634296.1:c.1812C>T
ENST00000634308.1:c.*1135C>T	ENSP00000489234.1:n.*1135C>T
ENST00000634620.1:n.4778C>T
ENST00000634810.1:n.3379C>T
ENST00000634844.1:c.3890C>T	ENSP00000489398.1:p.Pro1297Leu
NM_000053.3:c.4034C>T	NP_000044.2:p.Pro1345Leu
NM_001005918.2:c.3413C>T	NP_001005918.1:p.Pro1138Leu
NM_001243182.1:c.3701C>T	NP_001230111.1:p.Pro1234Leu
XM_005266423.2:c.3938C>T	XP_005266480.1:p.Pro1313Leu
XM_005266424.3:c.3938C>T	XP_005266481.1:p.Pro1313Leu
XM_005266427.2:c.3800C>T	XP_005266484.1:p.Pro1267Leu
XM_005266428.1:c.3782C>T	XP_005266485.1:p.Pro1261Leu
XM_005266430.3:c.4034C>T	XP_005266487.1:p.Pro1345Leu
XM_005266431.2:c.3998C>T	XP_005266488.1:p.Pro1333Leu
XM_005266432.2:c.3548C>T	XP_005266489.1:p.Pro1183Leu
XM_006719837.2:c.3938C>T	XP_006719900.1:p.Pro1313Leu
XM_006719838.1:c.1850C>T	XP_006719901.1:p.Pro617Leu
XM_006719839.1:c.1667C>T	XP_006719902.1:p.Pro556Leu
XM_011535117.1:c.3938C>T	XP_011533419.1:p.Pro1313Leu
XM_011535118.1:c.3899C>T	XP_011533420.1:p.Pro1300Leu
XM_011535119.1:c.3851C>T	XP_011533421.1:p.Pro1284Leu
XM_011535120.1:c.3620C>T	XP_011533422.1:p.Pro1207Leu
XM_011535121.1:c.3521C>T	XP_011533423.1:p.Pro1174Leu
XM_011535122.1:c.2702C>T	XP_011533424.1:p.Pro901Leu
XR_941601.1:n.4253C>T
XR_941602.1:n.4253C>T
XR_941603.1:n.4253C>T
XR_941604.1:n.4253C>T
NM_001330578.1:c.3800C>T	NP_001317507.1:p.Pro1267Leu
NM_001330579.1:c.3782C>T	NP_001317508.1:p.Pro1261Leu
XM_005266424.4:c.3938C>T	XP_005266481.1:p.Pro1313Leu
XM_005266430.4:c.4034C>T	XP_005266487.1:p.Pro1345Leu
XM_005266431.4:c.3998C>T	XP_005266488.1:p.Pro1333Leu
XM_006719837.3:c.3938C>T	XP_006719900.1:p.Pro1313Leu
XM_011535117.3:c.3938C>T	XP_011533419.1:p.Pro1313Leu
XM_017020627.1:c.3938C>T	XP_016876116.1:p.Pro1313Leu
NM_000053.4:c.4034C>T MANE Select	NP_000044.2:p.Pro1345Leu
NM_001005918.3:c.3413C>T	NP_001005918.1:p.Pro1138Leu
NM_001330579.2:c.3782C>T	NP_001317508.1:p.Pro1261Leu
NM_001243182.2:c.3701C>T	NP_001230111.1:p.Pro1234Leu
NM_001330578.2:c.3800C>T	NP_001317507.1:p.Pro1267Leu