Canonical Allele Identifier: CA483894926

Gene: ATP7B

Linked Data

• MyVariant Identifiers: chr13:g.52520501C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51946365C>A , CM000675.2:g.51946365C>A	GRCh38
NC_000013.10:g.52520501C>A , CM000675.1:g.52520501C>A	GRCh37
NC_000013.9:g.51418502C>A	NCBI36
NG_008806.1:g.70130G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*812G>T	ENSP00000489512.2:n.*812G>T
ENST00000673864.2:c.*1723G>T	ENSP00000501045.2:n.*1723G>T
ENST00000674147.2:c.2358G>T	ENSP00000500964.2:p.Thr786=
ENST00000242839.10:c.2979G>T MANE Select	ENSP00000242839.5:p.Thr993=
ENST00000344297.9:c.2358G>T	ENSP00000342559.5:p.Thr786=
ENST00000400366.6:c.2646G>T	ENSP00000383217.3:p.Thr882=
ENST00000448424.7:c.2727G>T	ENSP00000416738.3:p.Thr909=
ENST00000673772.1:c.2745G>T	ENSP00000501168.1:p.Thr915=
ENST00000673867.1:n.1126G>T
ENST00000674126.1:n.3342G>T
ENST00000674147.1:c.1914G>T	ENSP00000500964.1:p.Thr638=
ENST00000242839.8:c.2979G>T	ENSP00000242839.4:p.Thr993=
ENST00000344297.8:c.2358G>T	ENSP00000342559.5:p.Thr786=
ENST00000400366.5:c.2646G>T	ENSP00000383217.3:p.Thr882=
ENST00000400370.8:c.1689G>T	ENSP00000383221.3:p.Thr563=
ENST00000418097.7:c.2866-2074G>T	ENSP00000393343.2:n.2866-2074G>T
ENST00000448424.6:c.2745G>T	ENSP00000416738.2:p.Thr915=
ENST00000466629.1:n.199G>T
ENST00000634296.1:c.940G>T
ENST00000634308.1:c.*80G>T	ENSP00000489234.1:n.*80G>T
ENST00000634620.1:n.3723G>T
ENST00000634810.1:n.2324G>T
ENST00000634844.1:c.2835G>T	ENSP00000489398.1:p.Thr945=
ENST00000635406.1:n.325G>T
NM_000053.3:c.2979G>T	NP_000044.2:p.Thr993=
NM_001005918.2:c.2358G>T	NP_001005918.1:p.Thr786=
NM_001243182.1:c.2646G>T	NP_001230111.1:p.Thr882=
XM_005266423.2:c.2883G>T	XP_005266480.1:p.Thr961=
XM_005266424.3:c.2883G>T	XP_005266481.1:p.Thr961=
XM_005266427.2:c.2745G>T	XP_005266484.1:p.Thr915=
XM_005266428.1:c.2727G>T	XP_005266485.1:p.Thr909=
XM_005266430.3:c.2979G>T	XP_005266487.1:p.Thr993=
XM_005266431.2:c.2943G>T	XP_005266488.1:p.Thr981=
XM_005266432.2:c.2493G>T	XP_005266489.1:p.Thr831=
XM_006719837.2:c.2883G>T	XP_006719900.1:p.Thr961=
XM_006719838.1:c.795G>T	XP_006719901.1:p.Thr265=
XM_006719839.1:c.795G>T	XP_006719902.1:p.Thr265=
XM_011535117.1:c.2883G>T	XP_011533419.1:p.Thr961=
XM_011535118.1:c.2844G>T	XP_011533420.1:p.Thr948=
XM_011535119.1:c.2979G>T	XP_011533421.1:p.Thr993=
XM_011535120.1:c.2565G>T	XP_011533422.1:p.Thr855=
XM_011535121.1:c.2730+3642G>T	XP_011533423.1:n.2730+3642G>T
XM_011535122.1:c.1647G>T	XP_011533424.1:p.Thr549=
XR_941601.1:n.3198G>T
XR_941602.1:n.3198G>T
XR_941603.1:n.3198G>T
XR_941604.1:n.3198G>T
NM_001330578.1:c.2745G>T	NP_001317507.1:p.Thr915=
NM_001330579.1:c.2727G>T	NP_001317508.1:p.Thr909=
XM_005266424.4:c.2883G>T	XP_005266481.1:p.Thr961=
XM_005266430.4:c.2979G>T	XP_005266487.1:p.Thr993=
XM_005266431.4:c.2943G>T	XP_005266488.1:p.Thr981=
XM_006719837.3:c.2883G>T	XP_006719900.1:p.Thr961=
XM_011535117.3:c.2883G>T	XP_011533419.1:p.Thr961=
XM_017020627.1:c.2883G>T	XP_016876116.1:p.Thr961=
NM_000053.4:c.2979G>T MANE Select	NP_000044.2:p.Thr993=
NM_001005918.3:c.2358G>T	NP_001005918.1:p.Thr786=
NM_001330579.2:c.2727G>T	NP_001317508.1:p.Thr909=
NM_001243182.2:c.2646G>T	NP_001230111.1:p.Thr882=
NM_001330578.2:c.2745G>T	NP_001317507.1:p.Thr915=