Canonical Allele Identifier: CA2578217857

Gene: FGA

Linked Data

• dbSNP Id: rs2110819828
• gnomAD v4: 4-154589423-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154589423_154589424insT , CM000666.2:g.154589423_154589424insT	GRCh38
NC_000004.11:g.155510575_155510576insT , CM000666.1:g.155510575_155510576insT	GRCh37
NC_000004.10:g.155730025_155730026insT	NCBI36
NG_008832.1:g.6322_6323insA , LRG_557:g.6322_6323insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000651975.2:c.180+13_180+14insA	ENSP00000498441.1:n.180+13_180+14insA
ENST00000403106.8:c.180+13_180+14insA MANE Select	ENSP00000385981.3:n.180+13_180+14insA
ENST00000651975.1:c.180+13_180+14insA	ENSP00000498441.1:n.180+13_180+14insA
ENST00000302053.7:c.180+13_180+14insA	ENSP00000306361.3:n.180+13_180+14insA
ENST00000403106.7:c.180+13_180+14insA	ENSP00000385981.3:n.180+13_180+14insA
ENST00000622532.1:c.180+13_180+14insA	ENSP00000478487.1:n.180+13_180+14insA
NM_000508.3:c.180+13_180+14insA , LRG_557t1:c.180+13_180+14insA	NP_000499.1:n.180+13_180+14insA
NM_021871.2:c.180+13_180+14insA , LRG_557t2:c.180+13_180+14insA	NP_068657.1:n.180+13_180+14insA
NM_000508.4:c.180+13_180+14insA	NP_000499.1:n.180+13_180+14insA
NM_021871.3:c.180+13_180+14insA	NP_068657.1:n.180+13_180+14insA
NM_021871.4:c.180+13_180+14insA MANE Select	NP_068657.1:n.180+13_180+14insA
NM_000508.5:c.180+13_180+14insA	NP_000499.1:n.180+13_180+14insA