Canonical Allele Identifier: CA343805979
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs1403553441

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665664C>A , CM000663.2:g.172665664C>A GRCh38
NC_000001.10:g.172634804C>A , CM000663.1:g.172634804C>A GRCh37
NC_000001.9:g.170901427C>A NCBI36
NG_007269.1:g.11620C>A , LRG_58:g.11620C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.494C>A MANE Select ENSP00000356694.2:p.Thr165Asn
ENST00000340030.4:c.*64C>A ENSP00000344739.3:n.*64C>A
ENST00000367721.2:c.494C>A ENSP00000356694.2:p.Thr165Asn
NM_000639.2:c.494C>A NP_000630.1:p.Thr165Asn
NM_001302746.1:c.*64C>A NP_001289675.1:n.*64C>A
NM_000639.3:c.494C>A MANE Select NP_000630.1:p.Thr165Asn
NM_001302746.2:c.*64C>A NP_001289675.1:n.*64C>A