Canonical Allele Identifier: CA388031765

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52520429C>A (hg19) ; chr13:g.51946293C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946293C>A , CM000675.2:g.51946293C>A	GRCh38
NC_000013.10:g.52520429C>A , CM000675.1:g.52520429C>A	GRCh37
NC_000013.9:g.51418430C>A	NCBI36
NG_008806.1:g.70202G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*884G>T	ENSP00000489512.2:n.*884G>T
ENST00000673864.2:c.*1795G>T	ENSP00000501045.2:n.*1795G>T
ENST00000674147.2:c.2430G>T	ENSP00000500964.2:p.Met810Ile
ENST00000242839.10:c.3051G>T MANE Select	ENSP00000242839.5:p.Met1017Ile
ENST00000344297.9:c.2430G>T	ENSP00000342559.5:p.Met810Ile
ENST00000400366.6:c.2718G>T	ENSP00000383217.3:p.Met906Ile
ENST00000448424.7:c.2799G>T	ENSP00000416738.3:p.Met933Ile
ENST00000673772.1:c.2817G>T	ENSP00000501168.1:p.Met939Ile
ENST00000673867.1:n.1198G>T
ENST00000674126.1:n.3414G>T
ENST00000674147.1:c.1986G>T	ENSP00000500964.1:p.Met662Ile
ENST00000242839.8:c.3051G>T	ENSP00000242839.4:p.Met1017Ile
ENST00000344297.8:c.2430G>T	ENSP00000342559.5:p.Met810Ile
ENST00000400366.5:c.2718G>T	ENSP00000383217.3:p.Met906Ile
ENST00000400370.8:c.1761G>T	ENSP00000383221.3:p.Met587Ile
ENST00000418097.7:c.2866-2002G>T	ENSP00000393343.2:n.2866-2002G>T
ENST00000448424.6:c.2817G>T	ENSP00000416738.2:p.Met939Ile
ENST00000466629.1:n.271G>T
ENST00000634296.1:c.1012G>T
ENST00000634308.1:c.*152G>T	ENSP00000489234.1:n.*152G>T
ENST00000634620.1:n.3795G>T
ENST00000634810.1:n.2396G>T
ENST00000634844.1:c.2907G>T	ENSP00000489398.1:p.Met969Ile
ENST00000635406.1:n.397G>T
NM_000053.3:c.3051G>T	NP_000044.2:p.Met1017Ile
NM_001005918.2:c.2430G>T	NP_001005918.1:p.Met810Ile
NM_001243182.1:c.2718G>T	NP_001230111.1:p.Met906Ile
XM_005266423.2:c.2955G>T	XP_005266480.1:p.Met985Ile
XM_005266424.3:c.2955G>T	XP_005266481.1:p.Met985Ile
XM_005266427.2:c.2817G>T	XP_005266484.1:p.Met939Ile
XM_005266428.1:c.2799G>T	XP_005266485.1:p.Met933Ile
XM_005266430.3:c.3051G>T	XP_005266487.1:p.Met1017Ile
XM_005266431.2:c.3015G>T	XP_005266488.1:p.Met1005Ile
XM_005266432.2:c.2565G>T	XP_005266489.1:p.Met855Ile
XM_006719837.2:c.2955G>T	XP_006719900.1:p.Met985Ile
XM_006719838.1:c.867G>T	XP_006719901.1:p.Met289Ile
XM_006719839.1:c.867G>T	XP_006719902.1:p.Met289Ile
XM_011535117.1:c.2955G>T	XP_011533419.1:p.Met985Ile
XM_011535118.1:c.2916G>T	XP_011533420.1:p.Met972Ile
XM_011535119.1:c.3051G>T	XP_011533421.1:p.Met1017Ile
XM_011535120.1:c.2637G>T	XP_011533422.1:p.Met879Ile
XM_011535121.1:c.2730+3714G>T	XP_011533423.1:n.2730+3714G>T
XM_011535122.1:c.1719G>T	XP_011533424.1:p.Met573Ile
XR_941601.1:n.3270G>T
XR_941602.1:n.3270G>T
XR_941603.1:n.3270G>T
XR_941604.1:n.3270G>T
NM_001330578.1:c.2817G>T	NP_001317507.1:p.Met939Ile
NM_001330579.1:c.2799G>T	NP_001317508.1:p.Met933Ile
XM_005266424.4:c.2955G>T	XP_005266481.1:p.Met985Ile
XM_005266430.4:c.3051G>T	XP_005266487.1:p.Met1017Ile
XM_005266431.4:c.3015G>T	XP_005266488.1:p.Met1005Ile
XM_006719837.3:c.2955G>T	XP_006719900.1:p.Met985Ile
XM_011535117.3:c.2955G>T	XP_011533419.1:p.Met985Ile
XM_017020627.1:c.2955G>T	XP_016876116.1:p.Met985Ile
NM_000053.4:c.3051G>T MANE Select	NP_000044.2:p.Met1017Ile
NM_001005918.3:c.2430G>T	NP_001005918.1:p.Met810Ile
NM_001330579.2:c.2799G>T	NP_001317508.1:p.Met933Ile
NM_001243182.2:c.2718G>T	NP_001230111.1:p.Met906Ile
NM_001330578.2:c.2817G>T	NP_001317507.1:p.Met939Ile