Canonical Allele Identifier: CA1207431086
Gene: FASLG HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172664237T= , CM000663.2:g.172664237T= GRCh38
NC_000001.10:g.172633377T= , CM000663.1:g.172633377T= GRCh37
NC_000001.9:g.170900000T= NCBI36
NG_007269.1:g.10193T= , LRG_58:g.10193T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.395-97T= MANE Select ENSP00000356694.2:n.395-97T=
ENST00000340030.4:c.349-97T= ENSP00000344739.3:n.349-97T=
ENST00000367721.2:c.395-97T= ENSP00000356694.2:n.395-97T=
NM_000639.2:c.395-97T= NP_000630.1:n.395-97T=
NM_001302746.1:c.349-97T= NP_001289675.1:n.349-97T=
NM_000639.3:c.395-97T= MANE Select NP_000630.1:n.395-97T=
NM_001302746.2:c.349-97T= NP_001289675.1:n.349-97T=
Search 100 bp 5'
Search 100 bp 3'