Canonical Allele Identifier: CA2779393040
Gene: TNFRSF10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23222488T>A , CM000670.2:g.23222488T>A GRCh38
NC_000008.10:g.23080001T>A , CM000670.1:g.23080001T>A GRCh37
NC_000008.9:g.23135946T>A NCBI36
NG_032107.1:g.7680A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000221132.8:c.306+2268A>T MANE Select ENSP00000221132.3:n.306+2268A>T
ENST00000221132.7:c.306+2268A>T ENSP00000221132.3:n.306+2268A>T
ENST00000524158.5:c.-301+1945A>T ENSP00000428884.1:n.-301+1945A>T
ENST00000613472.1:c.31+2543A>T ENSP00000480778.1:n.31+2543A>T
NM_003844.3:c.306+2268A>T NP_003835.3:n.306+2268A>T
NM_003844.4:c.306+2268A>T MANE Select NP_003835.3:n.306+2268A>T
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