Canonical Allele Identifier: CA1009182354
Gene: FASLG HGNC NCBI

Linked Data

dbSNP Id: rs1659200485
gnomAD v3: 1-172664100-CATT-C
gnomAD v4: 1-172664100-CATT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172664103_172664105del , CM000663.2:g.172664103_172664105del GRCh38
NC_000001.10:g.172633243_172633245del , CM000663.1:g.172633243_172633245del GRCh37
NC_000001.9:g.170899866_170899868del NCBI36
NG_007269.1:g.10059_10061del , LRG_58:g.10059_10061del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.395-231_395-229del MANE Select ENSP00000356694.2:n.395-231_395-229del
ENST00000340030.4:c.349-231_349-229del ENSP00000344739.3:n.349-231_349-229del
ENST00000367721.2:c.395-231_395-229del ENSP00000356694.2:n.395-231_395-229del
NM_000639.2:c.395-231_395-229del NP_000630.1:n.395-231_395-229del
NM_001302746.1:c.349-231_349-229del NP_001289675.1:n.349-231_349-229del
NM_000639.3:c.395-231_395-229del MANE Select NP_000630.1:n.395-231_395-229del
NM_001302746.2:c.349-231_349-229del NP_001289675.1:n.349-231_349-229del
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