Canonical Allele Identifier: CA1207431059

Gene: FASLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172664154_172664155delinsGT , CM000663.2:g.172664154_172664155delinsGT	GRCh38
NC_000001.10:g.172633294_172633295delinsGT , CM000663.1:g.172633294_172633295delinsGT	GRCh37
NC_000001.9:g.170899917_170899918delinsGT	NCBI36
NG_007269.1:g.10110_10111delinsGT , LRG_58:g.10110_10111delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.395-180_395-179delinsGT MANE Select	ENSP00000356694.2:n.395-180_395-179delinsGT
ENST00000340030.4:c.349-180_349-179delinsGT	ENSP00000344739.3:n.349-180_349-179delinsGT
ENST00000367721.2:c.395-180_395-179delinsGT	ENSP00000356694.2:n.395-180_395-179delinsGT
NM_000639.2:c.395-180_395-179delinsGT	NP_000630.1:n.395-180_395-179delinsGT
NM_001302746.1:c.349-180_349-179delinsGT	NP_001289675.1:n.349-180_349-179delinsGT
NM_000639.3:c.395-180_395-179delinsGT MANE Select	NP_000630.1:n.395-180_395-179delinsGT
NM_001302746.2:c.349-180_349-179delinsGT	NP_001289675.1:n.349-180_349-179delinsGT