Canonical Allele Identifier: CA370568837

Gene: TNFRSF10A

Linked Data

• gnomAD v4: 8-23191835-G-T
• MyVariant Identifiers: chr8:g.23049348G>T (hg19) ; chr8:g.23191835G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23191835G>T , CM000670.2:g.23191835G>T	GRCh38
NC_000008.10:g.23049348G>T , CM000670.1:g.23049348G>T	GRCh37
NC_000008.9:g.23105293G>T	NCBI36
NG_032107.1:g.38333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.1266C>A MANE Select	ENSP00000221132.3:p.Asn422Lys
ENST00000221132.7:c.1266C>A	ENSP00000221132.3:p.Asn422Lys
ENST00000519862.1:n.321C>A
ENST00000613472.1:c.792C>A	ENSP00000480778.1:p.Asn264Lys
NM_003844.3:c.1266C>A	NP_003835.3:p.Asn422Lys
NM_003844.4:c.1266C>A MANE Select	NP_003835.3:p.Asn422Lys