Canonical Allele Identifier: CA1247577

Gene: FASLG

Linked Data

• dbSNP Id: rs372296143
• ExAC: 1:172634716 A / G
• gnomAD v2: 1-172634716-A-G
• gnomAD v3: 1-172665576-A-G
• gnomAD v4: 1-172665576-A-G
• MyVariant Identifiers: chr1:g.172634716A>G (hg19) ; chr1:g.172665576A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665576A>G , CM000663.2:g.172665576A>G	GRCh38
NC_000001.10:g.172634716A>G , CM000663.1:g.172634716A>G	GRCh37
NC_000001.9:g.170901339A>G	NCBI36
NG_007269.1:g.11532A>G , LRG_58:g.11532A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.452-46A>G MANE Select	ENSP00000356694.2:n.452-46A>G
ENST00000340030.4:c.*22-46A>G	ENSP00000344739.3:n.*22-46A>G
ENST00000367721.2:c.452-46A>G	ENSP00000356694.2:n.452-46A>G
NM_000639.2:c.452-46A>G	NP_000630.1:n.452-46A>G
NM_001302746.1:c.*22-46A>G	NP_001289675.1:n.*22-46A>G
NM_000639.3:c.452-46A>G MANE Select	NP_000630.1:n.452-46A>G
NM_001302746.2:c.*22-46A>G	NP_001289675.1:n.*22-46A>G