Canonical Allele Identifier: CA2746652314
Gene: FASLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665563C>G , CM000663.2:g.172665563C>G GRCh38
NC_000001.10:g.172634703C>G , CM000663.1:g.172634703C>G GRCh37
NC_000001.9:g.170901326C>G NCBI36
NG_007269.1:g.11519C>G , LRG_58:g.11519C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.452-59C>G MANE Select ENSP00000356694.2:n.452-59C>G
ENST00000340030.4:c.*22-59C>G ENSP00000344739.3:n.*22-59C>G
ENST00000367721.2:c.452-59C>G ENSP00000356694.2:n.452-59C>G
NM_000639.2:c.452-59C>G NP_000630.1:n.452-59C>G
NM_001302746.1:c.*22-59C>G NP_001289675.1:n.*22-59C>G
NM_000639.3:c.452-59C>G MANE Select NP_000630.1:n.452-59C>G
NM_001302746.2:c.*22-59C>G NP_001289675.1:n.*22-59C>G
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