Canonical Allele Identifier: CA1148725135
Gene: FASLG HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665695G= , CM000663.2:g.172665695G= GRCh38
NC_000001.10:g.172634835G= , CM000663.1:g.172634835G= GRCh37
NC_000001.9:g.170901458G= NCBI36
NG_007269.1:g.11651G= , LRG_58:g.11651G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.525G= MANE Select ENSP00000356694.2:p.Lys175=
ENST00000340030.4:c.*95G= ENSP00000344739.3:n.*95G=
ENST00000367721.2:c.525G= ENSP00000356694.2:p.Lys175=
NM_000639.2:c.525G= NP_000630.1:p.Lys175=
NM_001302746.1:c.*95G= NP_001289675.1:n.*95G=
NM_000639.3:c.525G= MANE Select NP_000630.1:p.Lys175=
NM_001302746.2:c.*95G= NP_001289675.1:n.*95G=
Search 100 bp 5'
Search 100 bp 3'