Canonical Allele Identifier: CA358526741
Gene: FGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154585702G>C , CM000666.2:g.154585702G>C GRCh38
NC_000004.11:g.155506854G>C , CM000666.1:g.155506854G>C GRCh37
NC_000004.10:g.155726304G>C NCBI36
NG_008832.1:g.10044C>G , LRG_557:g.10044C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651975.2:c.1727C>G ENSP00000498441.1:p.Ser576Cys
ENST00000403106.8:c.1727C>G MANE Select ENSP00000385981.3:p.Ser576Cys
ENST00000651975.1:c.1727C>G ENSP00000498441.1:p.Ser576Cys
ENST00000302053.7:c.1727C>G ENSP00000306361.3:p.Ser576Cys
ENST00000403106.7:c.1727C>G ENSP00000385981.3:p.Ser576Cys
ENST00000622532.1:c.652C>G ENSP00000478487.1:p.Leu218Val
NM_000508.3:c.1727C>G , LRG_557t1:c.1727C>G NP_000499.1:p.Ser576Cys
NM_021871.2:c.1727C>G , LRG_557t2:c.1727C>G NP_068657.1:p.Ser576Cys
NM_000508.4:c.1727C>G NP_000499.1:p.Ser576Cys
NM_021871.3:c.1727C>G NP_068657.1:p.Ser576Cys
NM_021871.4:c.1727C>G MANE Select NP_068657.1:p.Ser576Cys
NM_000508.5:c.1727C>G NP_000499.1:p.Ser576Cys