Canonical Allele Identifier: CA1247586
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs773263762

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665711C>T , CM000663.2:g.172665711C>T GRCh38
NC_000001.10:g.172634851C>T , CM000663.1:g.172634851C>T GRCh37
NC_000001.9:g.170901474C>T NCBI36
NG_007269.1:g.11667C>T , LRG_58:g.11667C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.541C>T MANE Select ENSP00000356694.2:p.Leu181Phe
ENST00000340030.4:c.*111C>T ENSP00000344739.3:n.*111C>T
ENST00000367721.2:c.541C>T ENSP00000356694.2:p.Leu181Phe
NM_000639.2:c.541C>T NP_000630.1:p.Leu181Phe
NM_001302746.1:c.*111C>T NP_001289675.1:n.*111C>T
NM_000639.3:c.541C>T MANE Select NP_000630.1:p.Leu181Phe
NM_001302746.2:c.*111C>T NP_001289675.1:n.*111C>T