Canonical Allele Identifier: CA4674552
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs766531884
ExAC: 8:23049295 G / T
gnomAD v2: 8-23049295-G-T
gnomAD v3: 8-23191782-G-T
gnomAD v4: 8-23191782-G-T
MyVariant Identifiers: chr8:g.23049295G>T (hg19) chr8:g.23191782G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191782G>T , CM000670.2:g.23191782G>T GRCh38
NC_000008.10:g.23049295G>T , CM000670.1:g.23049295G>T GRCh37
NC_000008.9:g.23105240G>T NCBI36
NG_032107.1:g.38386C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1319C>A MANE Select ENSP00000221132.3:p.Ala440Glu
ENST00000221132.7:c.1319C>A ENSP00000221132.3:p.Ala440Glu
ENST00000613472.1:c.845C>A ENSP00000480778.1:p.Ala282Glu
NM_003844.3:c.1319C>A NP_003835.3:p.Ala440Glu
NM_003844.4:c.1319C>A MANE Select NP_003835.3:p.Ala440Glu
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