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Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.85901164A>G , CM000685.2:g.85901164A>G
GRCh38
NC_000023.10:g.85156169A>G , CM000685.1:g.85156169A>G
GRCh37
NC_000023.9:g.85042825A>G
NCBI36
NG_009874.2:g.151399T>C , LRG_699:g.151399T>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000357749.7:c.1269T>C
MANE Select
ENSP00000350386.2:p.Phe423=
ENST00000357749.6:c.1269T>C
ENSP00000350386.2:p.Phe423=
ENST00000467744.2:n.127-38070T>C
NM_000390.2:c.1269T>C , LRG_699t1:c.1269T>C
NP_000381.1:p.Phe423=
XM_006724615.2:c.1206T>C
XP_006724678.1:p.Phe402=
XM_011530839.1:c.825T>C
XP_011529141.1:p.Phe275=
NM_000390.3:c.1269T>C
NP_000381.1:p.Phe423=
NM_001320959.1:c.825T>C
NP_001307888.1:p.Phe275=
NM_001362517.1:c.825T>C
NP_001349446.1:p.Phe275=
NM_001362518.1:c.825T>C
NP_001349447.1:p.Phe275=
NM_001362519.1:c.825T>C
NP_001349448.1:p.Phe275=
XM_017029242.2:c.1269T>C
XP_016884731.1:p.Phe423=
XM_017029246.1:c.825T>C
XP_016884735.1:p.Phe275=
XM_024452331.1:c.825T>C
XP_024308099.1:p.Phe275=
NM_000390.4:c.1269T>C
MANE Select
NP_000381.1:p.Phe423=
NM_001362518.2:c.825T>C
NP_001349447.1:p.Phe275=