Canonical Allele Identifier: CA649301550
Gene: FGA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154583796_154583797insA , CM000666.2:g.154583796_154583797insA GRCh38
NC_000004.11:g.155504948_155504949insA , CM000666.1:g.155504948_155504949insA GRCh37
NC_000004.10:g.155724398_155724399insA NCBI36
NG_008832.1:g.11949_11950insT , LRG_557:g.11949_11950insT

Transcript Alleles

HGVS Amino-acid change
ENST00000651975.2:c.*327_*328insT ENSP00000498441.1:n.*327_*328insT
ENST00000651975.1:c.*327_*328insT ENSP00000498441.1:n.*327_*328insT
ENST00000302053.7:c.*327_*328insT ENSP00000306361.3:n.*327_*328insT
NM_000508.3:c.*327_*328insT , LRG_557t1:c.*327_*328insT NP_000499.1:n.*327_*328insT
NM_000508.4:c.*327_*328insT NP_000499.1:n.*327_*328insT
NM_000508.5:c.*327_*328insT NP_000499.1:n.*327_*328insT