Canonical Allele Identifier: CA2649138019
Gene: FASLG HGNC NCBI

Linked Data

gnomAD v4: 1-172665555-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172665555C>A , CM000663.2:g.172665555C>A GRCh38
NC_000001.10:g.172634695C>A , CM000663.1:g.172634695C>A GRCh37
NC_000001.9:g.170901318C>A NCBI36
NG_007269.1:g.11511C>A , LRG_58:g.11511C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367721.3:c.452-67C>A MANE Select ENSP00000356694.2:n.452-67C>A
ENST00000340030.4:c.*22-67C>A ENSP00000344739.3:n.*22-67C>A
ENST00000367721.2:c.452-67C>A ENSP00000356694.2:n.452-67C>A
NM_000639.2:c.452-67C>A NP_000630.1:n.452-67C>A
NM_001302746.1:c.*22-67C>A NP_001289675.1:n.*22-67C>A
NM_000639.3:c.452-67C>A MANE Select NP_000630.1:n.452-67C>A
NM_001302746.2:c.*22-67C>A NP_001289675.1:n.*22-67C>A
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