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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.14158397T= , CM000665.2:g.14158397T=
GRCh38
NC_000003.11:g.14199897T= , CM000665.1:g.14199897T=
GRCh37
NC_000003.10:g.14174899T=
NCBI36
NG_011763.1:g.25276A= , LRG_472:g.25276A=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000285021.12:c.1486A=
MANE Select
ENSP00000285021.8:p.Ser496=
ENST00000285021.11:c.1486A=
ENSP00000285021.7:p.Ser496=
ENST00000476581.6:c.*939A=
ENSP00000424548.1:n.*939A=
NM_004628.4:c.1486A= , LRG_472t1:c.1486A=
NP_004619.3:p.Ser496=
NR_027299.1:n.1466A=
XM_011534092.1:c.1486A=
XP_011532394.1:p.Ser496=
XM_011534093.1:c.1486A=
XP_011532395.1:p.Ser496=
NM_001354726.1:c.907A=
NP_001341655.1:p.Ser303=
NM_001354727.1:c.1486A=
NP_001341656.1:p.Ser496=
NM_001354729.1:c.1468A=
NP_001341658.1:p.Ser490=
NM_001354730.1:c.1486A=
NP_001341659.1:p.Ser496=
NR_148950.1:n.1590A=
NR_148951.1:n.1466A=
XR_001740256.2:n.1519A=
XR_002959580.1:n.1519A=
XR_002959581.1:n.1519A=
NM_001354727.2:c.1486A=
NP_001341656.1:p.Ser496=
NM_004628.5:c.1486A=
MANE Select
NP_004619.3:p.Ser496=
NR_148950.2:n.1519A=
NR_148951.2:n.1395A=
NM_001354726.2:c.907A=
NP_001341655.1:p.Ser303=
NM_001354729.2:c.1468A=
NP_001341658.1:p.Ser490=
NM_001354730.2:c.1486A=
NP_001341659.1:p.Ser496=