Canonical Allele Identifier: CA1770754320
Gene: TNFRSF10A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.23191844_23191850delinsAGTTTTG , CM000670.2:g.23191844_23191850delinsAGTTTTG GRCh38
NC_000008.10:g.23049357_23049363delinsAGTTTTG , CM000670.1:g.23049357_23049363delinsAGTTTTG GRCh37
NC_000008.9:g.23105302_23105308delinsAGTTTTG NCBI36
NG_032107.1:g.38318_38324delinsCAAAACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000221132.8:c.1251_1257delinsCAAAACT MANE Select ENSP00000221132.3:p.Asn417=
ENST00000221132.7:c.1251_1257delinsCAAAACT ENSP00000221132.3:p.Asn417=
ENST00000519862.1:n.306_312delinsCAAAACT
ENST00000613472.1:c.777_783delinsCAAAACT ENSP00000480778.1:p.Asn259=
NM_003844.3:c.1251_1257delinsCAAAACT NP_003835.3:p.Asn417=
NM_003844.4:c.1251_1257delinsCAAAACT MANE Select NP_003835.3:p.Asn417=
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Search 100 bp 3'