Canonical Allele Identifier: CA343806294
Gene: FASLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665809G>T , CM000663.2:g.172665809G>T GRCh38
NC_000001.10:g.172634949G>T , CM000663.1:g.172634949G>T GRCh37
NC_000001.9:g.170901572G>T NCBI36
NG_007269.1:g.11765G>T , LRG_58:g.11765G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.639G>T MANE Select ENSP00000356694.2:p.Met213Ile
ENST00000340030.4:c.*209G>T ENSP00000344739.3:n.*209G>T
ENST00000367721.2:c.639G>T ENSP00000356694.2:p.Met213Ile
NM_000639.2:c.639G>T NP_000630.1:p.Met213Ile
NM_001302746.1:c.*209G>T NP_001289675.1:n.*209G>T
NM_000639.3:c.639G>T MANE Select NP_000630.1:p.Met213Ile
NM_001302746.2:c.*209G>T NP_001289675.1:n.*209G>T