Canonical Allele Identifier: CA343806042
Gene: FASLG HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.525G>C MANE Select ENSP00000356694.2:p.Lys175Asn
ENST00000340030.4:c.*95G>C ENSP00000344739.3:n.*95G>C
ENST00000367721.2:c.525G>C ENSP00000356694.2:p.Lys175Asn
NM_000639.2:c.525G>C NP_000630.1:p.Lys175Asn
NM_001302746.1:c.*95G>C NP_001289675.1:n.*95G>C
NM_000639.3:c.525G>C MANE Select NP_000630.1:p.Lys175Asn
NM_001302746.2:c.*95G>C NP_001289675.1:n.*95G>C