Canonical Allele Identifier: CA1770755841

Gene: TNFRSF10A

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.23212075_23212077delinsAAG , CM000670.2:g.23212075_23212077delinsAAG	GRCh38
NC_000008.10:g.23069588_23069590delinsAAG , CM000670.1:g.23069588_23069590delinsAAG	GRCh37
NC_000008.9:g.23125533_23125535delinsAAG	NCBI36
NG_032107.1:g.18091_18093delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000221132.8:c.403+39_403+41delinsCTT MANE Select	ENSP00000221132.3:n.403+39_403+41delinsCTT
ENST00000221132.7:c.403+39_403+41delinsCTT	ENSP00000221132.3:n.403+39_403+41delinsCTT
ENST00000524158.5:c.-204+39_-204+41delinsCTT	ENSP00000428884.1:n.-204+39_-204+41delinsCTT
ENST00000613472.1:c.32-9418_32-9416delinsCTT	ENSP00000480778.1:n.32-9418_32-9416delinsCTT
NM_003844.3:c.403+39_403+41delinsCTT	NP_003835.3:n.403+39_403+41delinsCTT
NM_003844.4:c.403+39_403+41delinsCTT MANE Select	NP_003835.3:n.403+39_403+41delinsCTT