Canonical Allele Identifier: CA173931906
Gene: TNFRSF10A HGNC NCBI

Linked Data

dbSNP Id: rs931943015
gnomAD v2: 8-23049357-A-C
gnomAD v3: 8-23191844-A-C
gnomAD v4: 8-23191844-A-C
MyVariant Identifiers: chr8:g.23049357A>C (hg19) chr8:g.23049357_23049363delinsCGTTTTG (hg19) chr8:g.23191844A>C (hg38) chr8:g.23191844_23191850delinsCGTTTTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191844A>C , CM000670.2:g.23191844A>C GRCh38
NC_000008.10:g.23049357A>C , CM000670.1:g.23049357A>C GRCh37
NC_000008.9:g.23105302A>C NCBI36
NG_032107.1:g.38324T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1257T>G MANE Select ENSP00000221132.3:p.Thr419=
ENST00000221132.7:c.1257T>G ENSP00000221132.3:p.Thr419=
ENST00000519862.1:n.312T>G
ENST00000613472.1:c.783T>G ENSP00000480778.1:p.Thr261=
NM_003844.3:c.1257T>G NP_003835.3:p.Thr419=
NM_003844.4:c.1257T>G MANE Select NP_003835.3:p.Thr419=
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