Canonical Allele Identifier: CA1207431045
Gene: FASLG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.172664122A= , CM000663.2:g.172664122A= GRCh38
NC_000001.10:g.172633262A= , CM000663.1:g.172633262A= GRCh37
NC_000001.9:g.170899885A= NCBI36
NG_007269.1:g.10078A= , LRG_58:g.10078A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367721.3:c.395-212A= MANE Select ENSP00000356694.2:n.395-212A=
ENST00000340030.4:c.349-212A= ENSP00000344739.3:n.349-212A=
ENST00000367721.2:c.395-212A= ENSP00000356694.2:n.395-212A=
NM_000639.2:c.395-212A= NP_000630.1:n.395-212A=
NM_001302746.1:c.349-212A= NP_001289675.1:n.349-212A=
NM_000639.3:c.395-212A= MANE Select NP_000630.1:n.395-212A=
NM_001302746.2:c.349-212A= NP_001289675.1:n.349-212A=
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