Canonical Allele Identifier: CA2649138028
Gene: FASLG HGNC NCBI

Linked Data

gnomAD v4: 1-172665574-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665574G>T , CM000663.2:g.172665574G>T GRCh38
NC_000001.10:g.172634714G>T , CM000663.1:g.172634714G>T GRCh37
NC_000001.9:g.170901337G>T NCBI36
NG_007269.1:g.11530G>T , LRG_58:g.11530G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.452-48G>T MANE Select ENSP00000356694.2:n.452-48G>T
ENST00000340030.4:c.*22-48G>T ENSP00000344739.3:n.*22-48G>T
ENST00000367721.2:c.452-48G>T ENSP00000356694.2:n.452-48G>T
NM_000639.2:c.452-48G>T NP_000630.1:n.452-48G>T
NM_001302746.1:c.*22-48G>T NP_001289675.1:n.*22-48G>T
NM_000639.3:c.452-48G>T MANE Select NP_000630.1:n.452-48G>T
NM_001302746.2:c.*22-48G>T NP_001289675.1:n.*22-48G>T
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