Canonical Allele Identifier: CA1207431615
Gene: FASLG HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665565T= , CM000663.2:g.172665565T= GRCh38
NC_000001.10:g.172634705T= , CM000663.1:g.172634705T= GRCh37
NC_000001.9:g.170901328T= NCBI36
NG_007269.1:g.11521T= , LRG_58:g.11521T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.452-57T= MANE Select ENSP00000356694.2:n.452-57T=
ENST00000340030.4:c.*22-57T= ENSP00000344739.3:n.*22-57T=
ENST00000367721.2:c.452-57T= ENSP00000356694.2:n.452-57T=
NM_000639.2:c.452-57T= NP_000630.1:n.452-57T=
NM_001302746.1:c.*22-57T= NP_001289675.1:n.*22-57T=
NM_000639.3:c.452-57T= MANE Select NP_000630.1:n.452-57T=
NM_001302746.2:c.*22-57T= NP_001289675.1:n.*22-57T=
Search 100 bp 5'
Search 100 bp 3'