Canonical Allele Identifier: CA10292221

Gene: TRMU

Linked Data

• dbSNP Id: rs748479934
• ExAC: 22:46748276 GCGTTTCAGCTCTGGGAGACTAGACCAGAGTTCCTGT / G
• gnomAD v2: 22-46748276-GCGTTTCAGCTCTGGGAGACTAGACCAGAGTTCCTGT-G
• gnomAD v3: 22-46352379-GCGTTTCAGCTCTGGGAGACTAGACCAGAGTTCCTGT-G
• gnomAD v4: 22-46352379-GCGTTTCAGCTCTGGGAGACTAGACCAGAGTTCCTGT-G
• MyVariant Identifiers: chr22:g.46748277_46748312del (hg19) ; chr22:g.46352380_46352415del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46352383_46352418del , CM000684.2:g.46352383_46352418del	GRCh38
NC_000022.10:g.46748280_46748315del , CM000684.1:g.46748280_46748315del	GRCh37
NC_000022.9:g.45126944_45126979del	NCBI36
NG_012173.1:g.21983_22018del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465378.6:n.873_908del
ENST00000642923.1:c.667+53_667+88del	ENSP00000494255.1:n.667+53_667+88del
ENST00000643137.1:c.667+53_667+88del	ENSP00000495331.1:n.667+53_667+88del
ENST00000644006.1:c.*216+53_*216+88del	ENSP00000493778.1:n.*216+53_*216+88del
ENST00000645026.1:n.823+53_823+88del
ENST00000645190.1:c.772+53_772+88del MANE Select	ENSP00000496496.1:n.772+53_772+88del
ENST00000647301.1:c.*216+53_*216+88del	ENSP00000496641.1:n.*216+53_*216+88del
ENST00000290846.8:c.772+53_772+88del	ENSP00000290846.4:n.772+53_772+88del
ENST00000381019.3:c.772+53_772+88del	ENSP00000370407.3:n.772+53_772+88del
ENST00000381021.7:c.*365+53_*365+88del	ENSP00000370409.3:n.*365+53_*365+88del
ENST00000441818.5:c.*306+53_*306+88del	ENSP00000393014.1:n.*306+53_*306+88del
ENST00000453630.5:c.*310+53_*310+88del	ENSP00000398488.1:n.*310+53_*310+88del
ENST00000456595.5:c.*306+53_*306+88del	ENSP00000413880.1:n.*306+53_*306+88del
ENST00000457572.5:c.*216+53_*216+88del	ENSP00000407700.1:n.*216+53_*216+88del
ENST00000463785.1:n.240+53_240+88del
NM_001282782.1:c.430+53_430+88del	NP_001269711.1:n.430+53_430+88del
NM_001282783.1:c.352+53_352+88del	NP_001269712.1:n.352+53_352+88del
NM_001282784.1:c.352+53_352+88del	NP_001269713.1:n.352+53_352+88del
NM_001282785.1:c.772+53_772+88del	NP_001269714.1:n.772+53_772+88del
NM_018006.4:c.772+53_772+88del	NP_060476.2:n.772+53_772+88del
NR_104240.1:n.1081+53_1081+88del
NR_104241.1:n.974+53_974+88del
XM_005261678.1:c.376+53_376+88del	XP_005261735.1:n.376+53_376+88del
XM_005261681.1:c.376+53_376+88del	XP_005261738.1:n.376+53_376+88del
XM_011530271.1:c.667+53_667+88del	XP_011528573.1:n.667+53_667+88del
XM_011530272.1:c.772+53_772+88del	XP_011528574.1:n.772+53_772+88del
XM_011530273.1:c.772+53_772+88del	XP_011528575.1:n.772+53_772+88del
XM_011530274.1:c.430+53_430+88del	XP_011528576.1:n.430+53_430+88del
XM_011530275.1:c.376+53_376+88del	XP_011528577.1:n.376+53_376+88del
XM_011530271.2:c.667+53_667+88del	XP_011528573.1:n.667+53_667+88del
XM_011530272.2:c.772+53_772+88del	XP_011528574.1:n.772+53_772+88del
XM_011530273.2:c.772+53_772+88del	XP_011528575.1:n.772+53_772+88del
XM_011530274.2:c.430+53_430+88del	XP_011528576.1:n.430+53_430+88del
XM_024452260.1:c.667+53_667+88del	XP_024308028.1:n.667+53_667+88del
XR_001755261.2:n.818+53_818+88del
XR_001755262.2:n.818+53_818+88del
NM_018006.5:c.772+53_772+88del MANE Select	NP_060476.2:n.772+53_772+88del
NM_001282782.2:c.430+53_430+88del	NP_001269711.1:n.430+53_430+88del
NM_001282783.2:c.352+53_352+88del	NP_001269712.1:n.352+53_352+88del
NM_001282784.2:c.352+53_352+88del	NP_001269713.1:n.352+53_352+88del
NM_001282785.2:c.772+53_772+88del	NP_001269714.1:n.772+53_772+88del
NR_104240.2:n.768+53_768+88del
NR_104241.2:n.661+53_661+88del