Canonical Allele Identifier: CA706123756

Gene: TOGARAM1

Linked Data

• dbSNP Id: rs1418919746
• gnomAD v3: 14-45073853-AACT-A
• gnomAD v4: 14-45073853-AACT-A
• MyVariant Identifiers: chr14:g.45543057_45543059del (hg19) ; chr14:g.45073854_45073856del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.45073856_45073858del , CM000676.2:g.45073856_45073858del	GRCh38
NC_000014.8:g.45543059_45543061del , CM000676.1:g.45543059_45543061del	GRCh37
NC_000014.7:g.44612809_44612811del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000361462.7:c.*295_*297del MANE Select	ENSP00000354917.2:n.*295_*297del
ENST00000361462.6:c.*295_*297del	ENSP00000354917.2:n.*295_*297del
ENST00000361577.7:c.*295_*297del	ENSP00000355045.3:n.*295_*297del
ENST00000557423.5:c.*2460_*2462del	ENSP00000451829.1:n.*2460_*2462del
NM_001308120.1:c.*295_*297del	NP_001295049.1:n.*295_*297del
NM_015091.2:c.*295_*297del	NP_055906.2:n.*295_*297del
NM_015091.3:c.*295_*297del	NP_055906.2:n.*295_*297del
NR_131765.1:n.5680_5682del
XM_011536571.1:c.*600_*602del	XP_011534873.1:n.*600_*602del
XM_017021098.1:c.*295_*297del	XP_016876587.1:n.*295_*297del
XM_017021099.1:c.*295_*297del	XP_016876588.1:n.*295_*297del
XR_001750194.1:n.5944_5946del
XR_001750195.1:n.5587_5589del
NM_001308120.2:c.*295_*297del MANE Select	NP_001295049.1:n.*295_*297del
NM_015091.4:c.*295_*297del	NP_055906.2:n.*295_*297del
NR_131765.2:n.5680_5682del