Canonical Allele Identifier: CA358526703
Gene: FGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154585696C>T , CM000666.2:g.154585696C>T GRCh38
NC_000004.11:g.155506848C>T , CM000666.1:g.155506848C>T GRCh37
NC_000004.10:g.155726298C>T NCBI36
NG_008832.1:g.10050G>A , LRG_557:g.10050G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000651975.2:c.1733G>A ENSP00000498441.1:p.Ser578Asn
ENST00000403106.8:c.1733G>A MANE Select ENSP00000385981.3:p.Ser578Asn
ENST00000651975.1:c.1733G>A ENSP00000498441.1:p.Ser578Asn
ENST00000302053.7:c.1733G>A ENSP00000306361.3:p.Ser578Asn
ENST00000403106.7:c.1733G>A ENSP00000385981.3:p.Ser578Asn
ENST00000622532.1:c.658G>A ENSP00000478487.1:p.Val220Ile
NM_000508.3:c.1733G>A , LRG_557t1:c.1733G>A NP_000499.1:p.Ser578Asn
NM_021871.2:c.1733G>A , LRG_557t2:c.1733G>A NP_068657.1:p.Ser578Asn
NM_000508.4:c.1733G>A NP_000499.1:p.Ser578Asn
NM_021871.3:c.1733G>A NP_068657.1:p.Ser578Asn
NM_021871.4:c.1733G>A MANE Select NP_068657.1:p.Ser578Asn
NM_000508.5:c.1733G>A NP_000499.1:p.Ser578Asn