Canonical Allele Identifier: CA6988496
Community Standard Title: NM_000053.4(ATP7B):c.4077G>T (p.Met1359Ile)
Gene: ATP7B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.51935640C>A , CM000675.2:g.51935640C>A GRCh38
NC_000013.10:g.52509776C>A , CM000675.1:g.52509776C>A GRCh37
NC_000013.9:g.51407777C>A NCBI36
NG_008806.1:g.80855G>T

Transcript Alleles

HGVS Amino-acid Change
NM_000053.4:c.4077G>T MANE Select NP_000044.2:p.Met1359Ile
ENST00000242839.10:c.4077G>T MANE Select ENSP00000242839.5:p.Met1359Ile
NM_000053.3:c.4077G>T NP_000044.2:p.Met1359Ile
NM_001005918.2:c.3456G>T NP_001005918.1:p.Met1152Ile
NM_001005918.3:c.3456G>T NP_001005918.1:p.Met1152Ile
NM_001243182.1:c.3744G>T NP_001230111.1:p.Met1248Ile
NM_001243182.2:c.3744G>T NP_001230111.1:p.Met1248Ile
NM_001330578.1:c.3843G>T NP_001317507.1:p.Met1281Ile
NM_001330578.2:c.3843G>T NP_001317507.1:p.Met1281Ile
NM_001330579.1:c.3825G>T NP_001317508.1:p.Met1275Ile
NM_001330579.2:c.3825G>T NP_001317508.1:p.Met1275Ile
ENST00000242839.8:c.4077G>T ENSP00000242839.4:p.Met1359Ile
ENST00000344297.8:c.3456G>T ENSP00000342559.5:p.Met1152Ile
ENST00000344297.9:c.3456G>T ENSP00000342559.5:p.Met1152Ile
ENST00000400366.5:c.3744G>T ENSP00000383217.3:p.Met1248Ile
ENST00000400366.6:c.3744G>T ENSP00000383217.3:p.Met1248Ile
ENST00000400370.8:c.2787G>T ENSP00000383221.3:p.Met929Ile
ENST00000418097.7:c.3882G>T ENSP00000393343.2:p.Met1294Ile
ENST00000448424.6:c.3843G>T ENSP00000416738.2:p.Met1281Ile
ENST00000448424.7:c.3825G>T ENSP00000416738.3:p.Met1275Ile
ENST00000634296.1:c.1855G>T
ENST00000634296.2:c.*1727G>T ENSP00000489512.2:n.*1727G>T
ENST00000634308.1:c.*1178G>T ENSP00000489234.1:n.*1178G>T
ENST00000634620.1:n.4821G>T
ENST00000634810.1:n.3422G>T
ENST00000634844.1:c.3933G>T ENSP00000489398.1:p.Met1311Ile
ENST00000673696.1:n.1400G>T
ENST00000673772.1:c.3843G>T ENSP00000501168.1:p.Met1281Ile
ENST00000673864.2:c.*2821G>T ENSP00000501045.2:n.*2821G>T
ENST00000673867.1:n.4216G>T
ENST00000673923.1:n.943G>T
ENST00000674147.1:c.3012G>T ENSP00000500964.1:p.Met1004Ile
ENST00000674147.2:c.3456G>T ENSP00000500964.2:p.Met1152Ile
XM_005266423.2:c.3981G>T XP_005266480.1:p.Met1327Ile
XM_005266424.3:c.3981G>T XP_005266481.1:p.Met1327Ile
XM_005266424.4:c.3981G>T XP_005266481.1:p.Met1327Ile
XM_005266427.2:c.3843G>T XP_005266484.1:p.Met1281Ile
XM_005266428.1:c.3825G>T XP_005266485.1:p.Met1275Ile
XM_005266430.3:c.4077G>T XP_005266487.1:p.Met1359Ile
XM_005266430.4:c.4077G>T XP_005266487.1:p.Met1359Ile
XM_005266431.2:c.4041G>T XP_005266488.1:p.Met1347Ile
XM_005266431.4:c.4041G>T XP_005266488.1:p.Met1347Ile
XM_005266432.2:c.3591G>T XP_005266489.1:p.Met1197Ile
XM_006719837.2:c.3981G>T XP_006719900.1:p.Met1327Ile
XM_006719837.3:c.3981G>T XP_006719900.1:p.Met1327Ile
XM_006719838.1:c.1893G>T XP_006719901.1:p.Met631Ile
XM_006719839.1:c.1710G>T XP_006719902.1:p.Met570Ile
XM_011535117.1:c.3981G>T XP_011533419.1:p.Met1327Ile
XM_011535117.3:c.3981G>T XP_011533419.1:p.Met1327Ile
XM_011535118.1:c.3942G>T XP_011533420.1:p.Met1314Ile
XM_011535119.1:c.3894G>T XP_011533421.1:p.Met1298Ile
XM_011535120.1:c.3663G>T XP_011533422.1:p.Met1221Ile
XM_011535121.1:c.3564G>T XP_011533423.1:p.Met1188Ile
XM_011535122.1:c.2745G>T XP_011533424.1:p.Met915Ile
XM_017020627.1:c.3981G>T XP_016876116.1:p.Met1327Ile
XR_941601.1:n.4296G>T
XR_941602.1:n.4296G>T
XR_941603.1:n.4296G>T
XR_941604.1:n.4296G>T