Canonical Allele Identifier: CA2799207852

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51974417_51974422del , CM000675.2:g.51974417_51974422del	GRCh38
NC_000013.10:g.52548553_52548558del , CM000675.1:g.52548553_52548558del	GRCh37
NC_000013.9:g.51446554_51446559del	NCBI36
NG_008806.1:g.42073_42078del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.798_803del	ENSP00000489512.2:p.Met266_Cys268delinsIle
ENST00000673864.2:c.798_803del	ENSP00000501045.2:p.Met266_Cys268delinsIle
ENST00000674147.2:c.798_803del	ENSP00000500964.2:p.Met266_Cys268delinsIle
ENST00000242839.10:c.798_803del MANE Select	ENSP00000242839.5:p.Met266_Cys268delinsIle
ENST00000344297.9:c.798_803del	ENSP00000342559.5:p.Met266_Cys268delinsIle
ENST00000400366.6:c.798_802+1del
ENST00000448424.7:c.798_803del	ENSP00000416738.3:p.Met266_Cys268delinsIle
ENST00000673772.1:c.798_803del	ENSP00000501168.1:p.Met266_Cys268delinsIle
ENST00000674078.1:n.903_908del
ENST00000674147.1:c.354_359del	ENSP00000500964.1:p.Met118_Cys120delinsIle
ENST00000242839.8:c.798_803del	ENSP00000242839.4:p.Met266_Cys268delinsIle
ENST00000344297.8:c.798_803del	ENSP00000342559.5:p.Met266_Cys268delinsIle
ENST00000400366.5:c.798_802+1del
ENST00000400370.8:c.798_803del	ENSP00000383221.3:p.Met266_Cys268delinsIle
ENST00000418097.7:c.798_803del	ENSP00000393343.2:p.Met266_Cys268delinsIle
ENST00000448424.6:c.798_803del	ENSP00000416738.2:p.Met266_Cys268delinsIle
ENST00000482841.6:n.919_924del
ENST00000634308.1:c.798_803del	ENSP00000489234.1:p.Met266_Cys268delinsIle
ENST00000634844.1:c.798_803del	ENSP00000489398.1:p.Met266_Cys268delinsIle
ENST00000635406.1:n.212-27944_212-27939del
NM_000053.3:c.798_803del	NP_000044.2:p.Met266_Cys268delinsIle
NM_001005918.2:c.798_803del	NP_001005918.1:p.Met266_Cys268delinsIle
NM_001243182.1:c.798_802+1del
XM_005266423.2:c.702_707del	XP_005266480.1:p.Met234_Cys236delinsIle
XM_005266424.3:c.702_707del	XP_005266481.1:p.Met234_Cys236delinsIle
XM_005266427.2:c.798_803del	XP_005266484.1:p.Met266_Cys268delinsIle
XM_005266428.1:c.798_803del	XP_005266485.1:p.Met266_Cys268delinsIle
XM_005266430.3:c.798_803del	XP_005266487.1:p.Met266_Cys268delinsIle
XM_005266431.2:c.762_767del	XP_005266488.1:p.Met254_Cys256delinsIle
XM_005266432.2:c.798_803del	XP_005266489.1:p.Met266_Cys268delinsIle
XM_006719837.2:c.702_707del	XP_006719900.1:p.Met234_Cys236delinsIle
XM_011535117.1:c.702_707del	XP_011533419.1:p.Met234_Cys236delinsIle
XM_011535118.1:c.798_803del	XP_011533420.1:p.Met266_Cys268delinsIle
XM_011535119.1:c.798_803del	XP_011533421.1:p.Met266_Cys268delinsIle
XM_011535120.1:c.798_803del	XP_011533422.1:p.Met266_Cys268delinsIle
XM_011535121.1:c.798_803del	XP_011533423.1:p.Met266_Cys268delinsIle
XR_941601.1:n.1017_1022del
XR_941602.1:n.1017_1022del
XR_941603.1:n.1017_1022del
XR_941604.1:n.1017_1022del
NM_001330578.1:c.798_803del	NP_001317507.1:p.Met266_Cys268delinsIle
NM_001330579.1:c.798_803del	NP_001317508.1:p.Met266_Cys268delinsIle
XM_005266424.4:c.702_707del	XP_005266481.1:p.Met234_Cys236delinsIle
XM_005266430.4:c.798_803del	XP_005266487.1:p.Met266_Cys268delinsIle
XM_005266431.4:c.762_767del	XP_005266488.1:p.Met254_Cys256delinsIle
XM_006719837.3:c.702_707del	XP_006719900.1:p.Met234_Cys236delinsIle
XM_011535117.3:c.702_707del	XP_011533419.1:p.Met234_Cys236delinsIle
XM_017020627.1:c.702_707del	XP_016876116.1:p.Met234_Cys236delinsIle
NM_000053.4:c.798_803del MANE Select	NP_000044.2:p.Met266_Cys268delinsIle
NM_001005918.3:c.798_803del	NP_001005918.1:p.Met266_Cys268delinsIle
NM_001330579.2:c.798_803del	NP_001317508.1:p.Met266_Cys268delinsIle
NM_001243182.2:c.798_802+1del
NM_001330578.2:c.798_803del	NP_001317507.1:p.Met266_Cys268delinsIle