Canonical Allele Identifier: CA10292266

Gene: TRMU

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.46353879G>A , CM000684.2:g.46353879G>A	GRCh38
NC_000022.10:g.46749776G>A , CM000684.1:g.46749776G>A	GRCh37
NC_000022.9:g.45128440G>A	NCBI36
NG_012173.1:g.23479G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642923.1:c.768+12G>A	ENSP00000494255.1:n.768+12G>A
ENST00000643137.1:c.768+12G>A	ENSP00000495331.1:n.768+12G>A
ENST00000644006.1:c.*317+12G>A	ENSP00000493778.1:n.*317+12G>A
ENST00000645026.1:n.936G>A
ENST00000645190.1:c.873+12G>A MANE Select	ENSP00000496496.1:n.873+12G>A
ENST00000647301.1:c.*317+12G>A	ENSP00000496641.1:n.*317+12G>A
ENST00000290846.8:c.873+12G>A	ENSP00000290846.4:n.873+12G>A
ENST00000381019.3:c.873+12G>A	ENSP00000370407.3:n.873+12G>A
ENST00000381021.7:c.*466+12G>A	ENSP00000370409.3:n.*466+12G>A
ENST00000441818.5:c.*407+12G>A	ENSP00000393014.1:n.*407+12G>A
ENST00000453630.5:c.*411+12G>A	ENSP00000398488.1:n.*411+12G>A
ENST00000456595.5:c.*407+12G>A	ENSP00000413880.1:n.*407+12G>A
ENST00000457572.5:c.*317+12G>A	ENSP00000407700.1:n.*317+12G>A
ENST00000485559.1:n.363G>A
ENST00000491612.1:n.1039+12G>A
NM_001282782.1:c.531+12G>A	NP_001269711.1:n.531+12G>A
NM_001282783.1:c.453+12G>A	NP_001269712.1:n.453+12G>A
NM_001282784.1:c.453+12G>A	NP_001269713.1:n.453+12G>A
NM_001282785.1:c.873+12G>A	NP_001269714.1:n.873+12G>A
NM_018006.4:c.873+12G>A	NP_060476.2:n.873+12G>A
NR_104240.1:n.1182+12G>A
NR_104241.1:n.1075+12G>A
XM_005261678.1:c.477+12G>A	XP_005261735.1:n.477+12G>A
XM_005261681.1:c.477+12G>A	XP_005261738.1:n.477+12G>A
XM_011530271.1:c.768+12G>A	XP_011528573.1:n.768+12G>A
XM_011530272.1:c.772+1549G>A	XP_011528574.1:n.772+1549G>A
XM_011530273.1:c.772+1549G>A	XP_011528575.1:n.772+1549G>A
XM_011530274.1:c.531+12G>A	XP_011528576.1:n.531+12G>A
XM_011530275.1:c.477+12G>A	XP_011528577.1:n.477+12G>A
XM_011530271.2:c.768+12G>A	XP_011528573.1:n.768+12G>A
XM_011530272.2:c.772+1549G>A	XP_011528574.1:n.772+1549G>A
XM_011530273.2:c.772+1549G>A	XP_011528575.1:n.772+1549G>A
XM_011530274.2:c.531+12G>A	XP_011528576.1:n.531+12G>A
XM_024452260.1:c.667+1549G>A	XP_024308028.1:n.667+1549G>A
XR_001755261.2:n.2173G>A
XR_001755262.2:n.2161+12G>A
NM_018006.5:c.873+12G>A MANE Select	NP_060476.2:n.873+12G>A
NM_001282782.2:c.531+12G>A	NP_001269711.1:n.531+12G>A
NM_001282783.2:c.453+12G>A	NP_001269712.1:n.453+12G>A
NM_001282784.2:c.453+12G>A	NP_001269713.1:n.453+12G>A
NM_001282785.2:c.873+12G>A	NP_001269714.1:n.873+12G>A
NR_104240.2:n.869+12G>A
NR_104241.2:n.762+12G>A