Canonical Allele Identifier: CA370583162
Gene: TNFRSF10A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23212143T>C , CM000670.2:g.23212143T>C GRCh38
NC_000008.10:g.23069656T>C , CM000670.1:g.23069656T>C GRCh37
NC_000008.9:g.23125601T>C NCBI36
NG_032107.1:g.18025A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.376A>G MANE Select ENSP00000221132.3:p.Ser126Gly
ENST00000221132.7:c.376A>G ENSP00000221132.3:p.Ser126Gly
ENST00000524158.5:c.-231A>G ENSP00000428884.1:n.-231A>G
ENST00000613472.1:c.32-9484A>G ENSP00000480778.1:n.32-9484A>G
NM_003844.3:c.376A>G NP_003835.3:p.Ser126Gly
NM_003844.4:c.376A>G MANE Select NP_003835.3:p.Ser126Gly