Canonical Allele Identifier: CA2649138021
Gene: FASLG HGNC NCBI

Linked Data

gnomAD v4: 1-172665562-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665562A>G , CM000663.2:g.172665562A>G GRCh38
NC_000001.10:g.172634702A>G , CM000663.1:g.172634702A>G GRCh37
NC_000001.9:g.170901325A>G NCBI36
NG_007269.1:g.11518A>G , LRG_58:g.11518A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.452-60A>G MANE Select ENSP00000356694.2:n.452-60A>G
ENST00000340030.4:c.*22-60A>G ENSP00000344739.3:n.*22-60A>G
ENST00000367721.2:c.452-60A>G ENSP00000356694.2:n.452-60A>G
NM_000639.2:c.452-60A>G NP_000630.1:n.452-60A>G
NM_001302746.1:c.*22-60A>G NP_001289675.1:n.*22-60A>G
NM_000639.3:c.452-60A>G MANE Select NP_000630.1:n.452-60A>G
NM_001302746.2:c.*22-60A>G NP_001289675.1:n.*22-60A>G
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