Canonical Allele Identifier: CA2649137864

Gene: FASLG

Linked Data

• gnomAD v4: 1-172664247-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172664247T>C , CM000663.2:g.172664247T>C	GRCh38
NC_000001.10:g.172633387T>C , CM000663.1:g.172633387T>C	GRCh37
NC_000001.9:g.170900010T>C	NCBI36
NG_007269.1:g.10203T>C , LRG_58:g.10203T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.395-87T>C MANE Select	ENSP00000356694.2:n.395-87T>C
ENST00000340030.4:c.349-87T>C	ENSP00000344739.3:n.349-87T>C
ENST00000367721.2:c.395-87T>C	ENSP00000356694.2:n.395-87T>C
NM_000639.2:c.395-87T>C	NP_000630.1:n.395-87T>C
NM_001302746.1:c.349-87T>C	NP_001289675.1:n.349-87T>C
NM_000639.3:c.395-87T>C MANE Select	NP_000630.1:n.395-87T>C
NM_001302746.2:c.349-87T>C	NP_001289675.1:n.349-87T>C