Canonical Allele Identifier: CA1154008006

Gene: TNFRSF1B

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12208645_12208648delinsAAGG , CM000663.2:g.12208645_12208648delinsAAGG	GRCh38
NC_000001.10:g.12268702_12268705delinsAAGG , CM000663.1:g.12268702_12268705delinsAAGG	GRCh37
NC_000001.9:g.12191289_12191292delinsAAGG	NCBI36
NG_029791.1:g.46643_46646delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.*1625_*1628delinsAAGG MANE Select	ENSP00000365435.3:n.*1625_*1628delinsAAGG
ENST00000376259.6:c.*1625_*1628delinsAAGG	ENSP00000365435.3:n.*1625_*1628delinsAAGG
ENST00000492361.1:n.3000_3003delinsAAGG
NM_001066.2:c.*1625_*1628delinsAAGG	NP_001057.1:n.*1625_*1628delinsAAGG
XM_011542060.1:c.*1625_*1628delinsAAGG	XP_011540362.1:n.*1625_*1628delinsAAGG
XM_011542061.1:c.*1625_*1628delinsAAGG	XP_011540363.1:n.*1625_*1628delinsAAGG
XM_011542062.1:c.3059_3062delinsAAGG	XP_011540364.1:n.3059_3062delinsAAGG
XM_011542063.1:c.*1625_*1628delinsAAGG	XP_011540365.1:n.*1625_*1628delinsAAGG
XM_011542060.2:c.*1625_*1628delinsAAGG	XP_011540362.1:n.*1625_*1628delinsAAGG
XM_011542063.2:c.*1625_*1628delinsAAGG	XP_011540365.1:n.*1625_*1628delinsAAGG
XM_017002214.1:c.*1625_*1628delinsAAGG	XP_016857703.1:n.*1625_*1628delinsAAGG
XM_017002215.1:c.*1625_*1628delinsAAGG	XP_016857704.1:n.*1625_*1628delinsAAGG
NM_001066.3:c.*1625_*1628delinsAAGG MANE Select	NP_001057.1:n.*1625_*1628delinsAAGG