Canonical Allele Identifier: CA1247469

Gene: FASLG

Linked Data

• ClinVar Variation Id: 293732
• ClinVar RCV Id: RCV000260218 ; RCV004021375
• dbSNP Id: rs375737004
• ExAC: 1:172628517 C / T
• gnomAD v2: 1-172628517-C-T
• gnomAD v3: 1-172659377-C-T
• gnomAD v4: 1-172659377-C-T
• MyVariant Identifiers: chr1:g.172628517C>T (hg19) ; chr1:g.172659377C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172659377C>T , CM000663.2:g.172659377C>T	GRCh38
NC_000001.10:g.172628517C>T , CM000663.1:g.172628517C>T	GRCh37
NC_000001.9:g.170895140C>T	NCBI36
NG_007269.1:g.5333C>T , LRG_58:g.5333C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.176C>T MANE Select	ENSP00000356694.2:p.Pro59Leu
ENST00000340030.4:c.176C>T	ENSP00000344739.3:p.Pro59Leu
ENST00000367721.2:c.176C>T	ENSP00000356694.2:p.Pro59Leu
NM_000639.2:c.176C>T	NP_000630.1:p.Pro59Leu
NM_001302746.1:c.176C>T	NP_001289675.1:p.Pro59Leu
NM_000639.3:c.176C>T MANE Select	NP_000630.1:p.Pro59Leu
NM_001302746.2:c.176C>T	NP_001289675.1:p.Pro59Leu