Canonical Allele Identifier: CA639832304

Gene: TRMU

Linked Data

• dbSNP Id: rs1388187153
• gnomAD v2: 22-46748122-GC-G
• MyVariant Identifiers: chr22:g.46748123del (hg19) ; chr22:g.46352226del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352227del , CM000684.2:g.46352227del	GRCh38
NC_000022.10:g.46748124del , CM000684.1:g.46748124del	GRCh37
NC_000022.9:g.45126788del	NCBI36
NG_012173.1:g.21827del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.754-37del
ENST00000642923.1:c.601-37del	ENSP00000494255.1:n.601-37del
ENST00000643137.1:c.601-37del	ENSP00000495331.1:n.601-37del
ENST00000644006.1:c.*150-37del	ENSP00000493778.1:n.*150-37del
ENST00000645026.1:n.757-37del
ENST00000645190.1:c.706-37del MANE Select	ENSP00000496496.1:n.706-37del
ENST00000647301.1:c.*150-37del	ENSP00000496641.1:n.*150-37del
ENST00000290846.8:c.706-37del	ENSP00000290846.4:n.706-37del
ENST00000381019.3:c.706-37del	ENSP00000370407.3:n.706-37del
ENST00000381021.7:c.*299-37del	ENSP00000370409.3:n.*299-37del
ENST00000441818.5:c.*240-37del	ENSP00000393014.1:n.*240-37del
ENST00000453630.5:c.*244-37del	ENSP00000398488.1:n.*244-37del
ENST00000456595.5:c.*240-37del	ENSP00000413880.1:n.*240-37del
ENST00000457572.5:c.*150-37del	ENSP00000407700.1:n.*150-37del
ENST00000463785.1:n.174-37del
ENST00000479648.1:n.526-37del
ENST00000485175.5:n.666-37del
ENST00000486620.5:n.748-37del
NM_001282782.1:c.364-37del	NP_001269711.1:n.364-37del
NM_001282783.1:c.286-37del	NP_001269712.1:n.286-37del
NM_001282784.1:c.286-37del	NP_001269713.1:n.286-37del
NM_001282785.1:c.706-37del	NP_001269714.1:n.706-37del
NM_018006.4:c.706-37del	NP_060476.2:n.706-37del
NR_104240.1:n.1015-37del
NR_104241.1:n.908-37del
XM_005261678.1:c.310-37del	XP_005261735.1:n.310-37del
XM_005261681.1:c.310-37del	XP_005261738.1:n.310-37del
XM_011530271.1:c.601-37del	XP_011528573.1:n.601-37del
XM_011530272.1:c.706-37del	XP_011528574.1:n.706-37del
XM_011530273.1:c.706-37del	XP_011528575.1:n.706-37del
XM_011530274.1:c.364-37del	XP_011528576.1:n.364-37del
XM_011530275.1:c.310-37del	XP_011528577.1:n.310-37del
XM_011530271.2:c.601-37del	XP_011528573.1:n.601-37del
XM_011530272.2:c.706-37del	XP_011528574.1:n.706-37del
XM_011530273.2:c.706-37del	XP_011528575.1:n.706-37del
XM_011530274.2:c.364-37del	XP_011528576.1:n.364-37del
XM_024452260.1:c.601-37del	XP_024308028.1:n.601-37del
XR_001755261.2:n.752-37del
XR_001755262.2:n.752-37del
NM_018006.5:c.706-37del MANE Select	NP_060476.2:n.706-37del
NM_001282782.2:c.364-37del	NP_001269711.1:n.364-37del
NM_001282783.2:c.286-37del	NP_001269712.1:n.286-37del
NM_001282784.2:c.286-37del	NP_001269713.1:n.286-37del
NM_001282785.2:c.706-37del	NP_001269714.1:n.706-37del
NR_104240.2:n.702-37del
NR_104241.2:n.595-37del