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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.173914562T= , CM000663.2:g.173914562T=
GRCh38
NC_000001.10:g.173883700T= , CM000663.1:g.173883700T=
GRCh37
NC_000001.9:g.172150323T=
NCBI36
NG_012462.1:g.7817A= , LRG_577:g.7817A=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000367698.4:c.399A=
MANE Select
ENSP00000356671.3:p.Gln133=
ENST00000367698.3:c.399A=
ENSP00000356671.3:p.Gln133=
ENST00000487183.1:n.104A=
ENST00000494024.1:n.625A=
ENST00000617423.4:c.399A=
ENSP00000478688.1:p.Gln133=
NM_000488.3:c.399A= , LRG_577t1:c.399A=
NP_000479.1:p.Gln133=
XM_005245198.2:c.255A=
XP_005245255.1:p.Gln85=
NM_001365052.1:c.255A=
NP_001351981.1:p.Gln85=
NM_000488.4:c.399A=
MANE Select
NP_000479.1:p.Gln133=
NM_001365052.2:c.255A=
NP_001351981.1:p.Gln85=
NM_001386302.1:c.399A=
NP_001373231.1:p.Gln133=
NM_001386303.1:c.480A=
NP_001373232.1:p.Gln160=
NM_001386304.1:c.399A=
NP_001373233.1:p.Gln133=
NM_001386305.1:c.399A=
NP_001373234.1:p.Gln133=
NM_001386306.1:c.399A=
NP_001373235.1:p.Gln133=