Canonical Allele Identifier: CA370568653

Gene: TNFRSF10A

Linked Data

• MyVariant Identifiers: chr8:g.23049325T>G (hg19) ; chr8:g.23191812T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23191812T>G , CM000670.2:g.23191812T>G	GRCh38
NC_000008.10:g.23049325T>G , CM000670.1:g.23049325T>G	GRCh37
NC_000008.9:g.23105270T>G	NCBI36
NG_032107.1:g.38356A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.1289A>C MANE Select	ENSP00000221132.3:p.Asp430Ala
ENST00000221132.7:c.1289A>C	ENSP00000221132.3:p.Asp430Ala
ENST00000613472.1:c.815A>C	ENSP00000480778.1:p.Asp272Ala
NM_003844.3:c.1289A>C	NP_003835.3:p.Asp430Ala
NM_003844.4:c.1289A>C MANE Select	NP_003835.3:p.Asp430Ala