Canonical Allele Identifier: CA343806022
Gene: FASLG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665685C>T , CM000663.2:g.172665685C>T GRCh38
NC_000001.10:g.172634825C>T , CM000663.1:g.172634825C>T GRCh37
NC_000001.9:g.170901448C>T NCBI36
NG_007269.1:g.11641C>T , LRG_58:g.11641C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.515C>T MANE Select ENSP00000356694.2:p.Ser172Phe
ENST00000340030.4:c.*85C>T ENSP00000344739.3:n.*85C>T
ENST00000367721.2:c.515C>T ENSP00000356694.2:p.Ser172Phe
NM_000639.2:c.515C>T NP_000630.1:p.Ser172Phe
NM_001302746.1:c.*85C>T NP_001289675.1:n.*85C>T
NM_000639.3:c.515C>T MANE Select NP_000630.1:p.Ser172Phe
NM_001302746.2:c.*85C>T NP_001289675.1:n.*85C>T