Canonical Allele Identifier: CA1770755832

Gene: TNFRSF10A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212072_23212074delinsGAA , CM000670.2:g.23212072_23212074delinsGAA	GRCh38
NC_000008.10:g.23069585_23069587delinsGAA , CM000670.1:g.23069585_23069587delinsGAA	GRCh37
NC_000008.9:g.23125530_23125532delinsGAA	NCBI36
NG_032107.1:g.18094_18096delinsTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.403+42_403+44delinsTTC MANE Select	ENSP00000221132.3:n.403+42_403+44delinsTTC
ENST00000221132.7:c.403+42_403+44delinsTTC	ENSP00000221132.3:n.403+42_403+44delinsTTC
ENST00000524158.5:c.-204+42_-204+44delinsTTC	ENSP00000428884.1:n.-204+42_-204+44delinsTTC
ENST00000613472.1:c.32-9415_32-9413delinsTTC	ENSP00000480778.1:n.32-9415_32-9413delinsTTC
NM_003844.3:c.403+42_403+44delinsTTC	NP_003835.3:n.403+42_403+44delinsTTC
NM_003844.4:c.403+42_403+44delinsTTC MANE Select	NP_003835.3:n.403+42_403+44delinsTTC