Canonical Allele Identifier: CA370568745

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23049338G>T (hg19) ; chr8:g.23191825G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23191825G>T , CM000670.2:g.23191825G>T	GRCh38
NC_000008.10:g.23049338G>T , CM000670.1:g.23049338G>T	GRCh37
NC_000008.9:g.23105283G>T	NCBI36
NG_032107.1:g.38343C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.1276C>A MANE Select	ENSP00000221132.3:p.His426Asn
ENST00000221132.7:c.1276C>A	ENSP00000221132.3:p.His426Asn
ENST00000519862.1:n.331C>A
ENST00000613472.1:c.802C>A	ENSP00000480778.1:p.His268Asn
NM_003844.3:c.1276C>A	NP_003835.3:p.His426Asn
NM_003844.4:c.1276C>A MANE Select	NP_003835.3:p.His426Asn