Canonical Allele Identifier: CA1504944964
Gene: FGA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154589208T= , CM000666.2:g.154589208T= GRCh38
NC_000004.11:g.155510360T= , CM000666.1:g.155510360T= GRCh37
NC_000004.10:g.155729810T= NCBI36
NG_008832.1:g.6538A= , LRG_557:g.6538A=

Transcript Alleles

HGVS Amino-acid change
ENST00000651975.2:c.180+229A= ENSP00000498441.1:n.180+229A=
ENST00000403106.8:c.180+229A= MANE Select ENSP00000385981.3:n.180+229A=
ENST00000651975.1:c.180+229A= ENSP00000498441.1:n.180+229A=
ENST00000302053.7:c.180+229A= ENSP00000306361.3:n.180+229A=
ENST00000403106.7:c.180+229A= ENSP00000385981.3:n.180+229A=
ENST00000622532.1:c.180+229A= ENSP00000478487.1:n.180+229A=
NM_000508.3:c.180+229A= , LRG_557t1:c.180+229A= NP_000499.1:n.180+229A=
NM_021871.2:c.180+229A= , LRG_557t2:c.180+229A= NP_068657.1:n.180+229A=
NM_000508.4:c.180+229A= NP_000499.1:n.180+229A=
NM_021871.3:c.180+229A= NP_068657.1:n.180+229A=
NM_021871.4:c.180+229A= MANE Select NP_068657.1:n.180+229A=
NM_000508.5:c.180+229A= NP_000499.1:n.180+229A=