Canonical Allele Identifier: CA6988780

Gene: ATP7B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.51944145G>A , CM000675.2:g.51944145G>A	GRCh38
NC_000013.10:g.52518281G>A , CM000675.1:g.52518281G>A	GRCh37
NC_000013.9:g.51416282G>A	NCBI36
NG_008806.1:g.72350C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000634296.2:c.*894-1591C>T	ENSP00000489512.2:n.*894-1591C>T
ENST00000673864.2:c.*1951C>T	ENSP00000501045.2:n.*1951C>T
ENST00000674147.2:c.2586C>T	ENSP00000500964.2:p.His862=
ENST00000242839.10:c.3207C>T MANE Select	ENSP00000242839.5:p.His1069=
ENST00000344297.9:c.2586C>T	ENSP00000342559.5:p.His862=
ENST00000400366.6:c.2874C>T	ENSP00000383217.3:p.His958=
ENST00000448424.7:c.2955C>T	ENSP00000416738.3:p.His985=
ENST00000673772.1:c.2973C>T	ENSP00000501168.1:p.His991=
ENST00000673867.1:n.3346C>T
ENST00000674126.1:n.3570C>T
ENST00000674147.1:c.2142C>T	ENSP00000500964.1:p.His714=
ENST00000242839.8:c.3207C>T	ENSP00000242839.4:p.His1069=
ENST00000344297.8:c.2586C>T	ENSP00000342559.5:p.His862=
ENST00000400366.5:c.2874C>T	ENSP00000383217.3:p.His958=
ENST00000400370.8:c.1917C>T	ENSP00000383221.3:p.His639=
ENST00000418097.7:c.3012C>T	ENSP00000393343.2:p.His1004=
ENST00000448424.6:c.2973C>T	ENSP00000416738.2:p.His991=
ENST00000466629.1:n.427C>T
ENST00000634296.1:c.1022-1591C>T
ENST00000634308.1:c.*308C>T	ENSP00000489234.1:n.*308C>T
ENST00000634620.1:n.3951C>T
ENST00000634810.1:n.2552C>T
ENST00000634844.1:c.3063C>T	ENSP00000489398.1:p.His1021=
NM_000053.3:c.3207C>T	NP_000044.2:p.His1069=
NM_001005918.2:c.2586C>T	NP_001005918.1:p.His862=
NM_001243182.1:c.2874C>T	NP_001230111.1:p.His958=
XM_005266423.2:c.3111C>T	XP_005266480.1:p.His1037=
XM_005266424.3:c.3111C>T	XP_005266481.1:p.His1037=
XM_005266427.2:c.2973C>T	XP_005266484.1:p.His991=
XM_005266428.1:c.2955C>T	XP_005266485.1:p.His985=
XM_005266430.3:c.3207C>T	XP_005266487.1:p.His1069=
XM_005266431.2:c.3171C>T	XP_005266488.1:p.His1057=
XM_005266432.2:c.2721C>T	XP_005266489.1:p.His907=
XM_006719837.2:c.3111C>T	XP_006719900.1:p.His1037=
XM_006719838.1:c.1023C>T	XP_006719901.1:p.His341=
XM_006719839.1:c.877-1591C>T	XP_006719902.1:n.877-1591C>T
XM_011535117.1:c.3111C>T	XP_011533419.1:p.His1037=
XM_011535118.1:c.3072C>T	XP_011533420.1:p.His1024=
XM_011535119.1:c.3061-1591C>T	XP_011533421.1:n.3061-1591C>T
XM_011535120.1:c.2793C>T	XP_011533422.1:p.His931=
XM_011535121.1:c.2731-1591C>T	XP_011533423.1:n.2731-1591C>T
XM_011535122.1:c.1875C>T	XP_011533424.1:p.His625=
XR_941601.1:n.3426C>T
XR_941602.1:n.3426C>T
XR_941603.1:n.3426C>T
XR_941604.1:n.3426C>T
NM_001330578.1:c.2973C>T	NP_001317507.1:p.His991=
NM_001330579.1:c.2955C>T	NP_001317508.1:p.His985=
XM_005266424.4:c.3111C>T	XP_005266481.1:p.His1037=
XM_005266430.4:c.3207C>T	XP_005266487.1:p.His1069=
XM_005266431.4:c.3171C>T	XP_005266488.1:p.His1057=
XM_006719837.3:c.3111C>T	XP_006719900.1:p.His1037=
XM_011535117.3:c.3111C>T	XP_011533419.1:p.His1037=
XM_017020627.1:c.3111C>T	XP_016876116.1:p.His1037=
NM_000053.4:c.3207C>T MANE Select	NP_000044.2:p.His1069=
NM_001005918.3:c.2586C>T	NP_001005918.1:p.His862=
NM_001330579.2:c.2955C>T	NP_001317508.1:p.His985=
NM_001243182.2:c.2874C>T	NP_001230111.1:p.His958=
NM_001330578.2:c.2973C>T	NP_001317507.1:p.His991=