Canonical Allele Identifier: CA388026153

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515256C>G (hg19) ; chr13:g.51941120C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941120C>G , CM000675.2:g.51941120C>G	GRCh38
NC_000013.10:g.52515256C>G , CM000675.1:g.52515256C>G	GRCh37
NC_000013.9:g.51413257C>G	NCBI36
NG_008806.1:g.75375G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1167G>C	ENSP00000489512.2:n.*1167G>C
ENST00000673864.2:c.*2261G>C	ENSP00000501045.2:n.*2261G>C
ENST00000674147.2:c.2896G>C	ENSP00000500964.2:p.Glu966Gln
ENST00000242839.10:c.3517G>C MANE Select	ENSP00000242839.5:p.Glu1173Gln
ENST00000344297.9:c.2896G>C	ENSP00000342559.5:p.Glu966Gln
ENST00000400366.6:c.3184G>C	ENSP00000383217.3:p.Glu1062Gln
ENST00000448424.7:c.3265G>C	ENSP00000416738.3:p.Glu1089Gln
ENST00000673772.1:c.3283G>C	ENSP00000501168.1:p.Glu1095Gln
ENST00000673867.1:n.3656G>C
ENST00000674126.1:n.3880G>C
ENST00000674147.1:c.2452G>C	ENSP00000500964.1:p.Glu818Gln
ENST00000242839.8:c.3517G>C	ENSP00000242839.4:p.Glu1173Gln
ENST00000344297.8:c.2896G>C	ENSP00000342559.5:p.Glu966Gln
ENST00000400366.5:c.3184G>C	ENSP00000383217.3:p.Glu1062Gln
ENST00000400370.8:c.2227G>C	ENSP00000383221.3:p.Glu743Gln
ENST00000418097.7:c.3322G>C	ENSP00000393343.2:p.Glu1108Gln
ENST00000448424.6:c.3283G>C	ENSP00000416738.2:p.Glu1095Gln
ENST00000634296.1:c.1295G>C
ENST00000634308.1:c.*618G>C	ENSP00000489234.1:n.*618G>C
ENST00000634620.1:n.4261G>C
ENST00000634810.1:n.2862G>C
ENST00000634844.1:c.3373G>C	ENSP00000489398.1:p.Glu1125Gln
NM_000053.3:c.3517G>C	NP_000044.2:p.Glu1173Gln
NM_001005918.2:c.2896G>C	NP_001005918.1:p.Glu966Gln
NM_001243182.1:c.3184G>C	NP_001230111.1:p.Glu1062Gln
XM_005266423.2:c.3421G>C	XP_005266480.1:p.Glu1141Gln
XM_005266424.3:c.3421G>C	XP_005266481.1:p.Glu1141Gln
XM_005266427.2:c.3283G>C	XP_005266484.1:p.Glu1095Gln
XM_005266428.1:c.3265G>C	XP_005266485.1:p.Glu1089Gln
XM_005266430.3:c.3517G>C	XP_005266487.1:p.Glu1173Gln
XM_005266431.2:c.3481G>C	XP_005266488.1:p.Glu1161Gln
XM_005266432.2:c.3031G>C	XP_005266489.1:p.Glu1011Gln
XM_006719837.2:c.3421G>C	XP_006719900.1:p.Glu1141Gln
XM_006719838.1:c.1333G>C	XP_006719901.1:p.Glu445Gln
XM_006719839.1:c.1150G>C	XP_006719902.1:p.Glu384Gln
XM_011535117.1:c.3421G>C	XP_011533419.1:p.Glu1141Gln
XM_011535118.1:c.3382G>C	XP_011533420.1:p.Glu1128Gln
XM_011535119.1:c.3334G>C	XP_011533421.1:p.Glu1112Gln
XM_011535120.1:c.3103G>C	XP_011533422.1:p.Glu1035Gln
XM_011535121.1:c.3004G>C	XP_011533423.1:p.Glu1002Gln
XM_011535122.1:c.2185G>C	XP_011533424.1:p.Glu729Gln
XR_941601.1:n.3736G>C
XR_941602.1:n.3736G>C
XR_941603.1:n.3736G>C
XR_941604.1:n.3736G>C
NM_001330578.1:c.3283G>C	NP_001317507.1:p.Glu1095Gln
NM_001330579.1:c.3265G>C	NP_001317508.1:p.Glu1089Gln
XM_005266424.4:c.3421G>C	XP_005266481.1:p.Glu1141Gln
XM_005266430.4:c.3517G>C	XP_005266487.1:p.Glu1173Gln
XM_005266431.4:c.3481G>C	XP_005266488.1:p.Glu1161Gln
XM_006719837.3:c.3421G>C	XP_006719900.1:p.Glu1141Gln
XM_011535117.3:c.3421G>C	XP_011533419.1:p.Glu1141Gln
XM_017020627.1:c.3421G>C	XP_016876116.1:p.Glu1141Gln
NM_000053.4:c.3517G>C MANE Select	NP_000044.2:p.Glu1173Gln
NM_001005918.3:c.2896G>C	NP_001005918.1:p.Glu966Gln
NM_001330579.2:c.3265G>C	NP_001317508.1:p.Glu1089Gln
NM_001243182.2:c.3184G>C	NP_001230111.1:p.Glu1062Gln
NM_001330578.2:c.3283G>C	NP_001317507.1:p.Glu1095Gln