Canonical Allele Identifier: CA388021157

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52511496G>C (hg19) ; chr13:g.51937360G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51937360G>C , CM000675.2:g.51937360G>C	GRCh38
NC_000013.10:g.52511496G>C , CM000675.1:g.52511496G>C	GRCh37
NC_000013.9:g.51409497G>C	NCBI36
NG_008806.1:g.79135C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000634296.2:c.*1587C>G	ENSP00000489512.2:n.*1587C>G
ENST00000673864.2:c.*2681C>G	ENSP00000501045.2:n.*2681C>G
ENST00000674147.2:c.3316C>G	ENSP00000500964.2:p.Leu1106Val
ENST00000242839.10:c.3937C>G MANE Select	ENSP00000242839.5:p.Leu1313Val
ENST00000344297.9:c.3316C>G	ENSP00000342559.5:p.Leu1106Val
ENST00000400366.6:c.3604C>G	ENSP00000383217.3:p.Leu1202Val
ENST00000448424.7:c.3685C>G	ENSP00000416738.3:p.Leu1229Val
ENST00000673696.1:n.1260C>G
ENST00000673772.1:c.3703C>G	ENSP00000501168.1:p.Leu1235Val
ENST00000673867.1:n.4076C>G
ENST00000673923.1:n.803C>G
ENST00000674147.1:c.2872C>G	ENSP00000500964.1:p.Leu958Val
ENST00000242839.8:c.3937C>G	ENSP00000242839.4:p.Leu1313Val
ENST00000344297.8:c.3316C>G	ENSP00000342559.5:p.Leu1106Val
ENST00000400366.5:c.3604C>G	ENSP00000383217.3:p.Leu1202Val
ENST00000400370.8:c.2647C>G	ENSP00000383221.3:p.Leu883Val
ENST00000418097.7:c.3742C>G	ENSP00000393343.2:p.Leu1248Val
ENST00000448424.6:c.3703C>G	ENSP00000416738.2:p.Leu1235Val
ENST00000634296.1:c.1715C>G
ENST00000634308.1:c.*1038C>G	ENSP00000489234.1:n.*1038C>G
ENST00000634620.1:n.4681C>G
ENST00000634810.1:n.3282C>G
ENST00000634844.1:c.3793C>G	ENSP00000489398.1:p.Leu1265Val
NM_000053.3:c.3937C>G	NP_000044.2:p.Leu1313Val
NM_001005918.2:c.3316C>G	NP_001005918.1:p.Leu1106Val
NM_001243182.1:c.3604C>G	NP_001230111.1:p.Leu1202Val
XM_005266423.2:c.3841C>G	XP_005266480.1:p.Leu1281Val
XM_005266424.3:c.3841C>G	XP_005266481.1:p.Leu1281Val
XM_005266427.2:c.3703C>G	XP_005266484.1:p.Leu1235Val
XM_005266428.1:c.3685C>G	XP_005266485.1:p.Leu1229Val
XM_005266430.3:c.3937C>G	XP_005266487.1:p.Leu1313Val
XM_005266431.2:c.3901C>G	XP_005266488.1:p.Leu1301Val
XM_005266432.2:c.3451C>G	XP_005266489.1:p.Leu1151Val
XM_006719837.2:c.3841C>G	XP_006719900.1:p.Leu1281Val
XM_006719838.1:c.1753C>G	XP_006719901.1:p.Leu585Val
XM_006719839.1:c.1570C>G	XP_006719902.1:p.Leu524Val
XM_011535117.1:c.3841C>G	XP_011533419.1:p.Leu1281Val
XM_011535118.1:c.3802C>G	XP_011533420.1:p.Leu1268Val
XM_011535119.1:c.3754C>G	XP_011533421.1:p.Leu1252Val
XM_011535120.1:c.3523C>G	XP_011533422.1:p.Leu1175Val
XM_011535121.1:c.3424C>G	XP_011533423.1:p.Leu1142Val
XM_011535122.1:c.2605C>G	XP_011533424.1:p.Leu869Val
XR_941601.1:n.4156C>G
XR_941602.1:n.4156C>G
XR_941603.1:n.4156C>G
XR_941604.1:n.4156C>G
NM_001330578.1:c.3703C>G	NP_001317507.1:p.Leu1235Val
NM_001330579.1:c.3685C>G	NP_001317508.1:p.Leu1229Val
XM_005266424.4:c.3841C>G	XP_005266481.1:p.Leu1281Val
XM_005266430.4:c.3937C>G	XP_005266487.1:p.Leu1313Val
XM_005266431.4:c.3901C>G	XP_005266488.1:p.Leu1301Val
XM_006719837.3:c.3841C>G	XP_006719900.1:p.Leu1281Val
XM_011535117.3:c.3841C>G	XP_011533419.1:p.Leu1281Val
XM_017020627.1:c.3841C>G	XP_016876116.1:p.Leu1281Val
NM_000053.4:c.3937C>G MANE Select	NP_000044.2:p.Leu1313Val
NM_001005918.3:c.3316C>G	NP_001005918.1:p.Leu1106Val
NM_001330579.2:c.3685C>G	NP_001317508.1:p.Leu1229Val
NM_001243182.2:c.3604C>G	NP_001230111.1:p.Leu1202Val
NM_001330578.2:c.3703C>G	NP_001317507.1:p.Leu1235Val