Canonical Allele Identifier: CA2799207360

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941470del , CM000675.2:g.51941470del	GRCh38
NC_000013.10:g.52515606del , CM000675.1:g.52515606del	GRCh37
NC_000013.9:g.51413607del	NCBI36
NG_008806.1:g.75027del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1063-244del	ENSP00000489512.2:n.*1063-244del
ENST00000673864.2:c.*2157-244del	ENSP00000501045.2:n.*2157-244del
ENST00000674147.2:c.2792-244del	ENSP00000500964.2:n.2792-244del
ENST00000242839.10:c.3413-244del MANE Select	ENSP00000242839.5:n.3413-244del
ENST00000344297.9:c.2792-244del	ENSP00000342559.5:n.2792-244del
ENST00000400366.6:c.3080-244del	ENSP00000383217.3:n.3080-244del
ENST00000448424.7:c.3161-244del	ENSP00000416738.3:n.3161-244del
ENST00000673772.1:c.3179-244del	ENSP00000501168.1:n.3179-244del
ENST00000673867.1:n.3552-244del
ENST00000674126.1:n.3776-244del
ENST00000674147.1:c.2348-244del	ENSP00000500964.1:n.2348-244del
ENST00000242839.8:c.3413-244del	ENSP00000242839.4:n.3413-244del
ENST00000344297.8:c.2792-244del	ENSP00000342559.5:n.2792-244del
ENST00000400366.5:c.3080-244del	ENSP00000383217.3:n.3080-244del
ENST00000400370.8:c.2123-244del	ENSP00000383221.3:n.2123-244del
ENST00000418097.7:c.3218-244del	ENSP00000393343.2:n.3218-244del
ENST00000448424.6:c.3179-244del	ENSP00000416738.2:n.3179-244del
ENST00000634296.1:c.1191-244del
ENST00000634308.1:c.*514-244del	ENSP00000489234.1:n.*514-244del
ENST00000634620.1:n.4157-244del
ENST00000634810.1:n.2758-244del
ENST00000634844.1:c.3269-244del	ENSP00000489398.1:n.3269-244del
NM_000053.3:c.3413-244del	NP_000044.2:n.3413-244del
NM_001005918.2:c.2792-244del	NP_001005918.1:n.2792-244del
NM_001243182.1:c.3080-244del	NP_001230111.1:n.3080-244del
XM_005266423.2:c.3317-244del	XP_005266480.1:n.3317-244del
XM_005266424.3:c.3317-244del	XP_005266481.1:n.3317-244del
XM_005266427.2:c.3179-244del	XP_005266484.1:n.3179-244del
XM_005266428.1:c.3161-244del	XP_005266485.1:n.3161-244del
XM_005266430.3:c.3413-244del	XP_005266487.1:n.3413-244del
XM_005266431.2:c.3377-244del	XP_005266488.1:n.3377-244del
XM_005266432.2:c.2927-244del	XP_005266489.1:n.2927-244del
XM_006719837.2:c.3317-244del	XP_006719900.1:n.3317-244del
XM_006719838.1:c.1229-244del	XP_006719901.1:n.1229-244del
XM_006719839.1:c.1046-244del	XP_006719902.1:n.1046-244del
XM_011535117.1:c.3317-244del	XP_011533419.1:n.3317-244del
XM_011535118.1:c.3278-244del	XP_011533420.1:n.3278-244del
XM_011535119.1:c.3230-244del	XP_011533421.1:n.3230-244del
XM_011535120.1:c.2999-244del	XP_011533422.1:n.2999-244del
XM_011535121.1:c.2900-244del	XP_011533423.1:n.2900-244del
XM_011535122.1:c.2081-244del	XP_011533424.1:n.2081-244del
XR_941601.1:n.3632-244del
XR_941602.1:n.3632-244del
XR_941603.1:n.3632-244del
XR_941604.1:n.3632-244del
NM_001330578.1:c.3179-244del	NP_001317507.1:n.3179-244del
NM_001330579.1:c.3161-244del	NP_001317508.1:n.3161-244del
XM_005266424.4:c.3317-244del	XP_005266481.1:n.3317-244del
XM_005266430.4:c.3413-244del	XP_005266487.1:n.3413-244del
XM_005266431.4:c.3377-244del	XP_005266488.1:n.3377-244del
XM_006719837.3:c.3317-244del	XP_006719900.1:n.3317-244del
XM_011535117.3:c.3317-244del	XP_011533419.1:n.3317-244del
XM_017020627.1:c.3317-244del	XP_016876116.1:n.3317-244del
NM_000053.4:c.3413-244del MANE Select	NP_000044.2:n.3413-244del
NM_001005918.3:c.2792-244del	NP_001005918.1:n.2792-244del
NM_001330579.2:c.3161-244del	NP_001317508.1:n.3161-244del
NM_001243182.2:c.3080-244del	NP_001230111.1:n.3080-244del
NM_001330578.2:c.3179-244del	NP_001317507.1:n.3179-244del