Canonical Allele Identifier: CA1247585
Gene: FASLG HGNC NCBI

Linked Data

ClinVar Variation Id: 1506314
dbSNP Id: rs772212573

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665702A>G , CM000663.2:g.172665702A>G GRCh38
NC_000001.10:g.172634842A>G , CM000663.1:g.172634842A>G GRCh37
NC_000001.9:g.170901465A>G NCBI36
NG_007269.1:g.11658A>G , LRG_58:g.11658A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.532A>G MANE Select ENSP00000356694.2:p.Lys178Glu
ENST00000340030.4:c.*102A>G ENSP00000344739.3:n.*102A>G
ENST00000367721.2:c.532A>G ENSP00000356694.2:p.Lys178Glu
NM_000639.2:c.532A>G NP_000630.1:p.Lys178Glu
NM_001302746.1:c.*102A>G NP_001289675.1:n.*102A>G
NM_000639.3:c.532A>G MANE Select NP_000630.1:p.Lys178Glu
NM_001302746.2:c.*102A>G NP_001289675.1:n.*102A>G