Canonical Allele Identifier: CA358533906
Community Standard Title: NM_021871.4(FGA):c.103C>G (p.Arg35Gly)
Gene: FGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154589514G>C , CM000666.2:g.154589514G>C GRCh38
NC_000004.11:g.155510666G>C , CM000666.1:g.155510666G>C GRCh37
NC_000004.10:g.155730116G>C NCBI36
NG_008832.1:g.6232C>G , LRG_557:g.6232C>G

Transcript Alleles

HGVS Amino-acid Change
NM_021871.4:c.103C>G MANE Select NP_068657.1:p.Arg35Gly
ENST00000403106.8:c.103C>G MANE Select ENSP00000385981.3:p.Arg35Gly
NM_000508.3:c.103C>G , LRG_557t1:c.103C>G NP_000499.1:p.Arg35Gly
NM_000508.4:c.103C>G NP_000499.1:p.Arg35Gly
NM_000508.5:c.103C>G NP_000499.1:p.Arg35Gly
NM_021871.2:c.103C>G , LRG_557t2:c.103C>G NP_068657.1:p.Arg35Gly
NM_021871.3:c.103C>G NP_068657.1:p.Arg35Gly
ENST00000302053.7:c.103C>G ENSP00000306361.3:p.Arg35Gly
ENST00000403106.7:c.103C>G ENSP00000385981.3:p.Arg35Gly
ENST00000622532.1:c.103C>G ENSP00000478487.1:p.Arg35Gly
ENST00000651975.1:c.103C>G ENSP00000498441.1:p.Arg35Gly
ENST00000651975.2:c.103C>G ENSP00000498441.1:p.Arg35Gly