Canonical Allele Identifier: CA388030098

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52518327C>A (hg19) ; chr13:g.51944191C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944191C>A , CM000675.2:g.51944191C>A	GRCh38
NC_000013.10:g.52518327C>A , CM000675.1:g.52518327C>A	GRCh37
NC_000013.9:g.51416328C>A	NCBI36
NG_008806.1:g.72304G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1637G>T	ENSP00000489512.2:n.*894-1637G>T
ENST00000673864.2:c.*1905G>T	ENSP00000501045.2:n.*1905G>T
ENST00000674147.2:c.2540G>T	ENSP00000500964.2:p.Arg847Met
ENST00000242839.10:c.3161G>T MANE Select	ENSP00000242839.5:p.Arg1054Met
ENST00000344297.9:c.2540G>T	ENSP00000342559.5:p.Arg847Met
ENST00000400366.6:c.2828G>T	ENSP00000383217.3:p.Arg943Met
ENST00000448424.7:c.2909G>T	ENSP00000416738.3:p.Arg970Met
ENST00000673772.1:c.2927G>T	ENSP00000501168.1:p.Arg976Met
ENST00000673867.1:n.3300G>T
ENST00000674126.1:n.3524G>T
ENST00000674147.1:c.2096G>T	ENSP00000500964.1:p.Arg699Met
ENST00000242839.8:c.3161G>T	ENSP00000242839.4:p.Arg1054Met
ENST00000344297.8:c.2540G>T	ENSP00000342559.5:p.Arg847Met
ENST00000400366.5:c.2828G>T	ENSP00000383217.3:p.Arg943Met
ENST00000400370.8:c.1871G>T	ENSP00000383221.3:p.Arg624Met
ENST00000418097.7:c.2966G>T	ENSP00000393343.2:p.Arg989Met
ENST00000448424.6:c.2927G>T	ENSP00000416738.2:p.Arg976Met
ENST00000466629.1:n.381G>T
ENST00000634296.1:c.1022-1637G>T
ENST00000634308.1:c.*262G>T	ENSP00000489234.1:n.*262G>T
ENST00000634620.1:n.3905G>T
ENST00000634810.1:n.2506G>T
ENST00000634844.1:c.3017G>T	ENSP00000489398.1:p.Arg1006Met
NM_000053.3:c.3161G>T	NP_000044.2:p.Arg1054Met
NM_001005918.2:c.2540G>T	NP_001005918.1:p.Arg847Met
NM_001243182.1:c.2828G>T	NP_001230111.1:p.Arg943Met
XM_005266423.2:c.3065G>T	XP_005266480.1:p.Arg1022Met
XM_005266424.3:c.3065G>T	XP_005266481.1:p.Arg1022Met
XM_005266427.2:c.2927G>T	XP_005266484.1:p.Arg976Met
XM_005266428.1:c.2909G>T	XP_005266485.1:p.Arg970Met
XM_005266430.3:c.3161G>T	XP_005266487.1:p.Arg1054Met
XM_005266431.2:c.3125G>T	XP_005266488.1:p.Arg1042Met
XM_005266432.2:c.2675G>T	XP_005266489.1:p.Arg892Met
XM_006719837.2:c.3065G>T	XP_006719900.1:p.Arg1022Met
XM_006719838.1:c.977G>T	XP_006719901.1:p.Arg326Met
XM_006719839.1:c.877-1637G>T	XP_006719902.1:n.877-1637G>T
XM_011535117.1:c.3065G>T	XP_011533419.1:p.Arg1022Met
XM_011535118.1:c.3026G>T	XP_011533420.1:p.Arg1009Met
XM_011535119.1:c.3061-1637G>T	XP_011533421.1:n.3061-1637G>T
XM_011535120.1:c.2747G>T	XP_011533422.1:p.Arg916Met
XM_011535121.1:c.2731-1637G>T	XP_011533423.1:n.2731-1637G>T
XM_011535122.1:c.1829G>T	XP_011533424.1:p.Arg610Met
XR_941601.1:n.3380G>T
XR_941602.1:n.3380G>T
XR_941603.1:n.3380G>T
XR_941604.1:n.3380G>T
NM_001330578.1:c.2927G>T	NP_001317507.1:p.Arg976Met
NM_001330579.1:c.2909G>T	NP_001317508.1:p.Arg970Met
XM_005266424.4:c.3065G>T	XP_005266481.1:p.Arg1022Met
XM_005266430.4:c.3161G>T	XP_005266487.1:p.Arg1054Met
XM_005266431.4:c.3125G>T	XP_005266488.1:p.Arg1042Met
XM_006719837.3:c.3065G>T	XP_006719900.1:p.Arg1022Met
XM_011535117.3:c.3065G>T	XP_011533419.1:p.Arg1022Met
XM_017020627.1:c.3065G>T	XP_016876116.1:p.Arg1022Met
NM_000053.4:c.3161G>T MANE Select	NP_000044.2:p.Arg1054Met
NM_001005918.3:c.2540G>T	NP_001005918.1:p.Arg847Met
NM_001330579.2:c.2909G>T	NP_001317508.1:p.Arg970Met
NM_001243182.2:c.2828G>T	NP_001230111.1:p.Arg943Met
NM_001330578.2:c.2927G>T	NP_001317507.1:p.Arg976Met