Canonical Allele Identifier: CA2695218140

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51974092_51974093insACA , CM000675.2:g.51974092_51974093insACA	GRCh38
NC_000013.10:g.52548228_52548229insACA , CM000675.1:g.52548228_52548229insACA	GRCh37
NC_000013.9:g.51446229_51446230insACA	NCBI36
NG_008806.1:g.42402_42403insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.1127_1128insTGT	ENSP00000489512.2:p.Ser376_Ile377insVal
ENST00000673864.2:c.1127_1128insTGT	ENSP00000501045.2:p.Ser376_Ile377insVal
ENST00000674147.2:c.1127_1128insTGT	ENSP00000500964.2:p.Ser376_Ile377insVal
ENST00000242839.10:c.1127_1128insTGT MANE Select	ENSP00000242839.5:p.Ser376_Ile377insVal
ENST00000344297.9:c.1127_1128insTGT	ENSP00000342559.5:p.Ser376_Ile377insVal
ENST00000400366.6:c.803-9_803-8insTGT	ENSP00000383217.3:n.803-9_803-8insTGT
ENST00000448424.7:c.1127_1128insTGT	ENSP00000416738.3:p.Ser376_Ile377insVal
ENST00000673772.1:c.1127_1128insTGT	ENSP00000501168.1:p.Ser376_Ile377insVal
ENST00000673789.1:n.83_84insTGT
ENST00000673864.1:c.83_84insTGT	ENSP00000501045.1:p.Ser28_Ile29insVal
ENST00000674078.1:n.1232_1233insTGT
ENST00000674147.1:c.683_684insTGT	ENSP00000500964.1:p.Ser228_Ile229insVal
ENST00000242839.8:c.1127_1128insTGT	ENSP00000242839.4:p.Ser376_Ile377insVal
ENST00000344297.8:c.1127_1128insTGT	ENSP00000342559.5:p.Ser376_Ile377insVal
ENST00000400366.5:c.803-9_803-8insTGT	ENSP00000383217.3:n.803-9_803-8insTGT
ENST00000400370.8:c.1127_1128insTGT	ENSP00000383221.3:p.Ser376_Ile377insVal
ENST00000418097.7:c.1127_1128insTGT	ENSP00000393343.2:p.Ser376_Ile377insVal
ENST00000448424.6:c.1127_1128insTGT	ENSP00000416738.2:p.Ser376_Ile377insVal
ENST00000482841.6:n.1248_1249insTGT
ENST00000634308.1:c.1127_1128insTGT	ENSP00000489234.1:p.Ser376_Ile377insVal
ENST00000634844.1:c.1127_1128insTGT	ENSP00000489398.1:p.Ser376_Ile377insVal
ENST00000635406.1:n.212-27615_212-27614insTGT
NM_000053.3:c.1127_1128insTGT	NP_000044.2:p.Ser376_Ile377insVal
NM_001005918.2:c.1127_1128insTGT	NP_001005918.1:p.Ser376_Ile377insVal
NM_001243182.1:c.803-9_803-8insTGT	NP_001230111.1:n.803-9_803-8insTGT
XM_005266423.2:c.1031_1032insTGT	XP_005266480.1:p.Ser344_Ile345insVal
XM_005266424.3:c.1031_1032insTGT	XP_005266481.1:p.Ser344_Ile345insVal
XM_005266427.2:c.1127_1128insTGT	XP_005266484.1:p.Ser376_Ile377insVal
XM_005266428.1:c.1127_1128insTGT	XP_005266485.1:p.Ser376_Ile377insVal
XM_005266430.3:c.1127_1128insTGT	XP_005266487.1:p.Ser376_Ile377insVal
XM_005266431.2:c.1091_1092insTGT	XP_005266488.1:p.Ser364_Ile365insVal
XM_005266432.2:c.1127_1128insTGT	XP_005266489.1:p.Ser376_Ile377insVal
XM_006719837.2:c.1031_1032insTGT	XP_006719900.1:p.Ser344_Ile345insVal
XM_011535117.1:c.1031_1032insTGT	XP_011533419.1:p.Ser344_Ile345insVal
XM_011535118.1:c.1127_1128insTGT	XP_011533420.1:p.Ser376_Ile377insVal
XM_011535119.1:c.1127_1128insTGT	XP_011533421.1:p.Ser376_Ile377insVal
XM_011535120.1:c.1127_1128insTGT	XP_011533422.1:p.Ser376_Ile377insVal
XM_011535121.1:c.1127_1128insTGT	XP_011533423.1:p.Ser376_Ile377insVal
XR_941601.1:n.1346_1347insTGT
XR_941602.1:n.1346_1347insTGT
XR_941603.1:n.1346_1347insTGT
XR_941604.1:n.1346_1347insTGT
NM_001330578.1:c.1127_1128insTGT	NP_001317507.1:p.Ser376_Ile377insVal
NM_001330579.1:c.1127_1128insTGT	NP_001317508.1:p.Ser376_Ile377insVal
XM_005266424.4:c.1031_1032insTGT	XP_005266481.1:p.Ser344_Ile345insVal
XM_005266430.4:c.1127_1128insTGT	XP_005266487.1:p.Ser376_Ile377insVal
XM_005266431.4:c.1091_1092insTGT	XP_005266488.1:p.Ser364_Ile365insVal
XM_006719837.3:c.1031_1032insTGT	XP_006719900.1:p.Ser344_Ile345insVal
XM_011535117.3:c.1031_1032insTGT	XP_011533419.1:p.Ser344_Ile345insVal
XM_017020627.1:c.1031_1032insTGT	XP_016876116.1:p.Ser344_Ile345insVal
NM_000053.4:c.1127_1128insTGT MANE Select	NP_000044.2:p.Ser376_Ile377insVal
NM_001005918.3:c.1127_1128insTGT	NP_001005918.1:p.Ser376_Ile377insVal
NM_001330579.2:c.1127_1128insTGT	NP_001317508.1:p.Ser376_Ile377insVal
NM_001243182.2:c.803-9_803-8insTGT	NP_001230111.1:n.803-9_803-8insTGT
NM_001330578.2:c.1127_1128insTGT	NP_001317507.1:p.Ser376_Ile377insVal