Canonical Allele Identifier: CA388031734
Gene: ATP7B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51946288T>A , CM000675.2:g.51946288T>A GRCh38
NC_000013.10:g.52520424T>A , CM000675.1:g.52520424T>A GRCh37
NC_000013.9:g.51418425T>A NCBI36
NG_008806.1:g.70207A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000634296.2:c.*889A>T ENSP00000489512.2:n.*889A>T
ENST00000673864.2:c.*1800A>T ENSP00000501045.2:n.*1800A>T
ENST00000674147.2:c.2435A>T ENSP00000500964.2:p.His812Leu
ENST00000242839.10:c.3056A>T MANE Select ENSP00000242839.5:p.His1019Leu
ENST00000344297.9:c.2435A>T ENSP00000342559.5:p.His812Leu
ENST00000400366.6:c.2723A>T ENSP00000383217.3:p.His908Leu
ENST00000448424.7:c.2804A>T ENSP00000416738.3:p.His935Leu
ENST00000673772.1:c.2822A>T ENSP00000501168.1:p.His941Leu
ENST00000673867.1:n.1203A>T
ENST00000674126.1:n.3419A>T
ENST00000674147.1:c.1991A>T ENSP00000500964.1:p.His664Leu
ENST00000242839.8:c.3056A>T ENSP00000242839.4:p.His1019Leu
ENST00000344297.8:c.2435A>T ENSP00000342559.5:p.His812Leu
ENST00000400366.5:c.2723A>T ENSP00000383217.3:p.His908Leu
ENST00000400370.8:c.1766A>T ENSP00000383221.3:p.His589Leu
ENST00000418097.7:c.2866-1997A>T ENSP00000393343.2:n.2866-1997A>T
ENST00000448424.6:c.2822A>T ENSP00000416738.2:p.His941Leu
ENST00000466629.1:n.276A>T
ENST00000634296.1:c.1017A>T
ENST00000634308.1:c.*157A>T ENSP00000489234.1:n.*157A>T
ENST00000634620.1:n.3800A>T
ENST00000634810.1:n.2401A>T
ENST00000634844.1:c.2912A>T ENSP00000489398.1:p.His971Leu
ENST00000635406.1:n.402A>T
NM_000053.3:c.3056A>T NP_000044.2:p.His1019Leu
NM_001005918.2:c.2435A>T NP_001005918.1:p.His812Leu
NM_001243182.1:c.2723A>T NP_001230111.1:p.His908Leu
XM_005266423.2:c.2960A>T XP_005266480.1:p.His987Leu
XM_005266424.3:c.2960A>T XP_005266481.1:p.His987Leu
XM_005266427.2:c.2822A>T XP_005266484.1:p.His941Leu
XM_005266428.1:c.2804A>T XP_005266485.1:p.His935Leu
XM_005266430.3:c.3056A>T XP_005266487.1:p.His1019Leu
XM_005266431.2:c.3020A>T XP_005266488.1:p.His1007Leu
XM_005266432.2:c.2570A>T XP_005266489.1:p.His857Leu
XM_006719837.2:c.2960A>T XP_006719900.1:p.His987Leu
XM_006719838.1:c.872A>T XP_006719901.1:p.His291Leu
XM_006719839.1:c.872A>T XP_006719902.1:p.His291Leu
XM_011535117.1:c.2960A>T XP_011533419.1:p.His987Leu
XM_011535118.1:c.2921A>T XP_011533420.1:p.His974Leu
XM_011535119.1:c.3056A>T XP_011533421.1:p.His1019Leu
XM_011535120.1:c.2642A>T XP_011533422.1:p.His881Leu
XM_011535121.1:c.2730+3719A>T XP_011533423.1:n.2730+3719A>T
XM_011535122.1:c.1724A>T XP_011533424.1:p.His575Leu
XR_941601.1:n.3275A>T
XR_941602.1:n.3275A>T
XR_941603.1:n.3275A>T
XR_941604.1:n.3275A>T
NM_001330578.1:c.2822A>T NP_001317507.1:p.His941Leu
NM_001330579.1:c.2804A>T NP_001317508.1:p.His935Leu
XM_005266424.4:c.2960A>T XP_005266481.1:p.His987Leu
XM_005266430.4:c.3056A>T XP_005266487.1:p.His1019Leu
XM_005266431.4:c.3020A>T XP_005266488.1:p.His1007Leu
XM_006719837.3:c.2960A>T XP_006719900.1:p.His987Leu
XM_011535117.3:c.2960A>T XP_011533419.1:p.His987Leu
XM_017020627.1:c.2960A>T XP_016876116.1:p.His987Leu
NM_000053.4:c.3056A>T MANE Select NP_000044.2:p.His1019Leu
NM_001005918.3:c.2435A>T NP_001005918.1:p.His812Leu
NM_001330579.2:c.2804A>T NP_001317508.1:p.His935Leu
NM_001243182.2:c.2723A>T NP_001230111.1:p.His908Leu
NM_001330578.2:c.2822A>T NP_001317507.1:p.His941Leu