Canonical Allele Identifier: CA483894179

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52515341G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51941205G>A , CM000675.2:g.51941205G>A	GRCh38
NC_000013.10:g.52515341G>A , CM000675.1:g.52515341G>A	GRCh37
NC_000013.9:g.51413342G>A	NCBI36
NG_008806.1:g.75290C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*1082C>T	ENSP00000489512.2:n.*1082C>T
ENST00000673864.2:c.*2176C>T	ENSP00000501045.2:n.*2176C>T
ENST00000674147.2:c.2811C>T	ENSP00000500964.2:p.Phe937=
ENST00000242839.10:c.3432C>T MANE Select	ENSP00000242839.5:p.Phe1144=
ENST00000344297.9:c.2811C>T	ENSP00000342559.5:p.Phe937=
ENST00000400366.6:c.3099C>T	ENSP00000383217.3:p.Phe1033=
ENST00000448424.7:c.3180C>T	ENSP00000416738.3:p.Phe1060=
ENST00000673772.1:c.3198C>T	ENSP00000501168.1:p.Phe1066=
ENST00000673867.1:n.3571C>T
ENST00000674126.1:n.3795C>T
ENST00000674147.1:c.2367C>T	ENSP00000500964.1:p.Phe789=
ENST00000242839.8:c.3432C>T	ENSP00000242839.4:p.Phe1144=
ENST00000344297.8:c.2811C>T	ENSP00000342559.5:p.Phe937=
ENST00000400366.5:c.3099C>T	ENSP00000383217.3:p.Phe1033=
ENST00000400370.8:c.2142C>T	ENSP00000383221.3:p.Phe714=
ENST00000418097.7:c.3237C>T	ENSP00000393343.2:p.Phe1079=
ENST00000448424.6:c.3198C>T	ENSP00000416738.2:p.Phe1066=
ENST00000634296.1:c.1210C>T
ENST00000634308.1:c.*533C>T	ENSP00000489234.1:n.*533C>T
ENST00000634620.1:n.4176C>T
ENST00000634810.1:n.2777C>T
ENST00000634844.1:c.3288C>T	ENSP00000489398.1:p.Phe1096=
NM_000053.3:c.3432C>T	NP_000044.2:p.Phe1144=
NM_001005918.2:c.2811C>T	NP_001005918.1:p.Phe937=
NM_001243182.1:c.3099C>T	NP_001230111.1:p.Phe1033=
XM_005266423.2:c.3336C>T	XP_005266480.1:p.Phe1112=
XM_005266424.3:c.3336C>T	XP_005266481.1:p.Phe1112=
XM_005266427.2:c.3198C>T	XP_005266484.1:p.Phe1066=
XM_005266428.1:c.3180C>T	XP_005266485.1:p.Phe1060=
XM_005266430.3:c.3432C>T	XP_005266487.1:p.Phe1144=
XM_005266431.2:c.3396C>T	XP_005266488.1:p.Phe1132=
XM_005266432.2:c.2946C>T	XP_005266489.1:p.Phe982=
XM_006719837.2:c.3336C>T	XP_006719900.1:p.Phe1112=
XM_006719838.1:c.1248C>T	XP_006719901.1:p.Phe416=
XM_006719839.1:c.1065C>T	XP_006719902.1:p.Phe355=
XM_011535117.1:c.3336C>T	XP_011533419.1:p.Phe1112=
XM_011535118.1:c.3297C>T	XP_011533420.1:p.Phe1099=
XM_011535119.1:c.3249C>T	XP_011533421.1:p.Phe1083=
XM_011535120.1:c.3018C>T	XP_011533422.1:p.Phe1006=
XM_011535121.1:c.2919C>T	XP_011533423.1:p.Phe973=
XM_011535122.1:c.2100C>T	XP_011533424.1:p.Phe700=
XR_941601.1:n.3651C>T
XR_941602.1:n.3651C>T
XR_941603.1:n.3651C>T
XR_941604.1:n.3651C>T
NM_001330578.1:c.3198C>T	NP_001317507.1:p.Phe1066=
NM_001330579.1:c.3180C>T	NP_001317508.1:p.Phe1060=
XM_005266424.4:c.3336C>T	XP_005266481.1:p.Phe1112=
XM_005266430.4:c.3432C>T	XP_005266487.1:p.Phe1144=
XM_005266431.4:c.3396C>T	XP_005266488.1:p.Phe1132=
XM_006719837.3:c.3336C>T	XP_006719900.1:p.Phe1112=
XM_011535117.3:c.3336C>T	XP_011533419.1:p.Phe1112=
XM_017020627.1:c.3336C>T	XP_016876116.1:p.Phe1112=
NM_000053.4:c.3432C>T MANE Select	NP_000044.2:p.Phe1144=
NM_001005918.3:c.2811C>T	NP_001005918.1:p.Phe937=
NM_001330579.2:c.3180C>T	NP_001317508.1:p.Phe1060=
NM_001243182.2:c.3099C>T	NP_001230111.1:p.Phe1033=
NM_001330578.2:c.3198C>T	NP_001317507.1:p.Phe1066=