Canonical Allele Identifier: CA2519817625

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208743dup , CM000663.2:g.12208743dup	GRCh38
NC_000001.10:g.12268800dup , CM000663.1:g.12268800dup	GRCh37
NC_000001.9:g.12191387dup	NCBI36
NG_029791.1:g.46741dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1723dup MANE Select	ENSP00000365435.3:n.*1723dup
ENST00000376259.6:c.*1723dup	ENSP00000365435.3:n.*1723dup
ENST00000492361.1:n.3098dup
NM_001066.2:c.*1723dup	NP_001057.1:n.*1723dup
XM_011542060.1:c.*1723dup	XP_011540362.1:n.*1723dup
XM_011542061.1:c.*1723dup	XP_011540363.1:n.*1723dup
XM_011542062.1:c.3157dup	XP_011540364.1:n.3157dup
XM_011542063.1:c.*1723dup	XP_011540365.1:n.*1723dup
XM_011542060.2:c.*1723dup	XP_011540362.1:n.*1723dup
XM_011542063.2:c.*1723dup	XP_011540365.1:n.*1723dup
XM_017002214.1:c.*1723dup	XP_016857703.1:n.*1723dup
XM_017002215.1:c.*1723dup	XP_016857704.1:n.*1723dup
NM_001066.3:c.*1723dup MANE Select	NP_001057.1:n.*1723dup