Canonical Allele Identifier: CA1207431613

Gene: FASLG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665563_172665567delinsCTTAG , CM000663.2:g.172665563_172665567delinsCTTAG	GRCh38
NC_000001.10:g.172634703_172634707delinsCTTAG , CM000663.1:g.172634703_172634707delinsCTTAG	GRCh37
NC_000001.9:g.170901326_170901330delinsCTTAG	NCBI36
NG_007269.1:g.11519_11523delinsCTTAG , LRG_58:g.11519_11523delinsCTTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.452-59_452-55delinsCTTAG MANE Select	ENSP00000356694.2:n.452-59_452-55delinsCTTAG
ENST00000340030.4:c.*22-59_*22-55delinsCTTAG	ENSP00000344739.3:n.*22-59_*22-55delinsCTTAG
ENST00000367721.2:c.452-59_452-55delinsCTTAG	ENSP00000356694.2:n.452-59_452-55delinsCTTAG
NM_000639.2:c.452-59_452-55delinsCTTAG	NP_000630.1:n.452-59_452-55delinsCTTAG
NM_001302746.1:c.*22-59_*22-55delinsCTTAG	NP_001289675.1:n.*22-59_*22-55delinsCTTAG
NM_000639.3:c.452-59_452-55delinsCTTAG MANE Select	NP_000630.1:n.452-59_452-55delinsCTTAG
NM_001302746.2:c.*22-59_*22-55delinsCTTAG	NP_001289675.1:n.*22-59_*22-55delinsCTTAG