Canonical Allele Identifier: CA2643340360

Gene: TNFRSF1B

Linked Data

• gnomAD v4: 1-12192846-GCCTCCT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.12192855_12192860del , CM000663.2:g.12192855_12192860del	GRCh38
NC_000001.10:g.12252912_12252917del , CM000663.1:g.12252912_12252917del	GRCh37
NC_000001.9:g.12175499_12175504del	NCBI36
NG_029791.1:g.30853_30858del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376259.7:c.552-8_552-3del MANE Select	ENSP00000365435.3:n.552-8_552-3del
ENST00000376259.6:c.552-8_552-3del	ENSP00000365435.3:n.552-8_552-3del
ENST00000489921.1:n.264-8_264-3del
ENST00000492361.1:n.541-8_541-3del
NM_001066.2:c.552-8_552-3del	NP_001057.1:n.552-8_552-3del
XM_011542060.1:c.552-8_552-3del	XP_011540362.1:n.552-8_552-3del
XM_011542061.1:c.552-8_552-3del	XP_011540363.1:n.552-8_552-3del
XM_011542062.1:c.531-8_531-3del	XP_011540364.1:n.531-8_531-3del
XM_011542063.1:c.552-8_552-3del	XP_011540365.1:n.552-8_552-3del
XM_011542060.2:c.552-8_552-3del	XP_011540362.1:n.552-8_552-3del
XM_011542063.2:c.552-8_552-3del	XP_011540365.1:n.552-8_552-3del
XM_017002211.1:c.552-8_552-3del	XP_016857700.1:n.552-8_552-3del
XM_017002214.1:c.-34-8_-34-3del	XP_016857703.1:n.-34-8_-34-3del
XM_017002215.1:c.-34-8_-34-3del	XP_016857704.1:n.-34-8_-34-3del
NM_001066.3:c.552-8_552-3del MANE Select	NP_001057.1:n.552-8_552-3del