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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.173909628G= , CM000663.2:g.173909628G=
GRCh38
NC_000001.10:g.173878766G= , CM000663.1:g.173878766G=
GRCh37
NC_000001.9:g.172145389G=
NCBI36
NG_012462.1:g.12751C= , LRG_577:g.12751C=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000367698.4:c.1077C=
MANE Select
ENSP00000356671.3:p.Asp359=
ENST00000367698.3:c.1077C=
ENSP00000356671.3:p.Asp359=
ENST00000617423.4:c.560-2135C=
ENSP00000478688.1:n.560-2135C=
NM_000488.3:c.1077C= , LRG_577t1:c.1077C=
NP_000479.1:p.Asp359=
XM_005245198.2:c.933C=
XP_005245255.1:p.Asp311=
NM_001365052.1:c.933C=
NP_001351981.1:p.Asp311=
NM_000488.4:c.1077C=
MANE Select
NP_000479.1:p.Asp359=
NM_001365052.2:c.933C=
NP_001351981.1:p.Asp311=
NM_001386302.1:c.1200C=
NP_001373231.1:p.Asp400=
NM_001386303.1:c.1158C=
NP_001373232.1:p.Asp386=
NM_001386304.1:c.1056C=
NP_001373233.1:p.Asp352=
NM_001386305.1:c.1020C=
NP_001373234.1:p.Asp340=
NM_001386306.1:c.861C=
NP_001373235.1:p.Asp287=