Canonical Allele Identifier: CA2695218782

Gene: ATP7B

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941099del , CM000675.2:g.51941099del	GRCh38
NC_000013.10:g.52515235del , CM000675.1:g.52515235del	GRCh37
NC_000013.9:g.51413236del	NCBI36
NG_008806.1:g.75396del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1188del	ENSP00000489512.2:n.*1188del
ENST00000673864.2:c.*2282del	ENSP00000501045.2:n.*2282del
ENST00000674147.2:c.2917del	ENSP00000500964.2:p.Ile973SerfsTer12
ENST00000242839.10:c.3538del MANE Select	ENSP00000242839.5:p.Ile1180SerfsTer12
ENST00000344297.9:c.2917del	ENSP00000342559.5:p.Ile973SerfsTer12
ENST00000400366.6:c.3205del	ENSP00000383217.3:p.Ile1069SerfsTer12
ENST00000448424.7:c.3286del	ENSP00000416738.3:p.Ile1096SerfsTer12
ENST00000673772.1:c.3304del	ENSP00000501168.1:p.Ile1102SerfsTer12
ENST00000673867.1:n.3677del
ENST00000674126.1:n.3901del
ENST00000674147.1:c.2473del	ENSP00000500964.1:p.Ile825SerfsTer12
ENST00000242839.8:c.3538del	ENSP00000242839.4:p.Ile1180SerfsTer12
ENST00000344297.8:c.2917del	ENSP00000342559.5:p.Ile973SerfsTer12
ENST00000400366.5:c.3205del	ENSP00000383217.3:p.Ile1069SerfsTer12
ENST00000400370.8:c.2248del	ENSP00000383221.3:p.Ile750SerfsTer12
ENST00000418097.7:c.3343del	ENSP00000393343.2:p.Ile1115SerfsTer12
ENST00000448424.6:c.3304del	ENSP00000416738.2:p.Ile1102SerfsTer12
ENST00000634296.1:c.1316del
ENST00000634308.1:c.*639del	ENSP00000489234.1:n.*639del
ENST00000634620.1:n.4282del
ENST00000634810.1:n.2883del
ENST00000634844.1:c.3394del	ENSP00000489398.1:p.Ile1132SerfsTer12
NM_000053.3:c.3538del	NP_000044.2:p.Ile1180SerfsTer12
NM_001005918.2:c.2917del	NP_001005918.1:p.Ile973SerfsTer12
NM_001243182.1:c.3205del	NP_001230111.1:p.Ile1069SerfsTer12
XM_005266423.2:c.3442del	XP_005266480.1:p.Ile1148SerfsTer12
XM_005266424.3:c.3442del	XP_005266481.1:p.Ile1148SerfsTer12
XM_005266427.2:c.3304del	XP_005266484.1:p.Ile1102SerfsTer12
XM_005266428.1:c.3286del	XP_005266485.1:p.Ile1096SerfsTer12
XM_005266430.3:c.3538del	XP_005266487.1:p.Ile1180SerfsTer12
XM_005266431.2:c.3502del	XP_005266488.1:p.Ile1168SerfsTer12
XM_005266432.2:c.3052del	XP_005266489.1:p.Ile1018SerfsTer12
XM_006719837.2:c.3442del	XP_006719900.1:p.Ile1148SerfsTer12
XM_006719838.1:c.1354del	XP_006719901.1:p.Ile452SerfsTer12
XM_006719839.1:c.1171del	XP_006719902.1:p.Ile391SerfsTer12
XM_011535117.1:c.3442del	XP_011533419.1:p.Ile1148SerfsTer12
XM_011535118.1:c.3403del	XP_011533420.1:p.Ile1135SerfsTer12
XM_011535119.1:c.3355del	XP_011533421.1:p.Ile1119SerfsTer12
XM_011535120.1:c.3124del	XP_011533422.1:p.Ile1042SerfsTer12
XM_011535121.1:c.3025del	XP_011533423.1:p.Ile1009SerfsTer12
XM_011535122.1:c.2206del	XP_011533424.1:p.Ile736SerfsTer12
XR_941601.1:n.3757del
XR_941602.1:n.3757del
XR_941603.1:n.3757del
XR_941604.1:n.3757del
NM_001330578.1:c.3304del	NP_001317507.1:p.Ile1102SerfsTer12
NM_001330579.1:c.3286del	NP_001317508.1:p.Ile1096SerfsTer12
XM_005266424.4:c.3442del	XP_005266481.1:p.Ile1148SerfsTer12
XM_005266430.4:c.3538del	XP_005266487.1:p.Ile1180SerfsTer12
XM_005266431.4:c.3502del	XP_005266488.1:p.Ile1168SerfsTer12
XM_006719837.3:c.3442del	XP_006719900.1:p.Ile1148SerfsTer12
XM_011535117.3:c.3442del	XP_011533419.1:p.Ile1148SerfsTer12
XM_017020627.1:c.3442del	XP_016876116.1:p.Ile1148SerfsTer12
NM_000053.4:c.3538del MANE Select	NP_000044.2:p.Ile1180SerfsTer12
NM_001005918.3:c.2917del	NP_001005918.1:p.Ile973SerfsTer12
NM_001330579.2:c.3286del	NP_001317508.1:p.Ile1096SerfsTer12
NM_001243182.2:c.3205del	NP_001230111.1:p.Ile1069SerfsTer12
NM_001330578.2:c.3304del	NP_001317507.1:p.Ile1102SerfsTer12