Canonical Allele Identifier: CA1207431614

Gene: FASLG

Linked Data

• dbSNP Id: rs1659239940
• gnomAD v4: 1-172665563-CTTAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.172665566_172665569del , CM000663.2:g.172665566_172665569del	GRCh38
NC_000001.10:g.172634706_172634709del , CM000663.1:g.172634706_172634709del	GRCh37
NC_000001.9:g.170901329_170901332del	NCBI36
NG_007269.1:g.11522_11525del , LRG_58:g.11522_11525del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367721.3:c.452-56_452-53del MANE Select	ENSP00000356694.2:n.452-56_452-53del
ENST00000340030.4:c.*22-56_*22-53del	ENSP00000344739.3:n.*22-56_*22-53del
ENST00000367721.2:c.452-56_452-53del	ENSP00000356694.2:n.452-56_452-53del
NM_000639.2:c.452-56_452-53del	NP_000630.1:n.452-56_452-53del
NM_001302746.1:c.*22-56_*22-53del	NP_001289675.1:n.*22-56_*22-53del
NM_000639.3:c.452-56_452-53del MANE Select	NP_000630.1:n.452-56_452-53del
NM_001302746.2:c.*22-56_*22-53del	NP_001289675.1:n.*22-56_*22-53del