Canonical Allele Identifier: CA2141037409
Gene: TRMT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60975676T= , CM000676.2:g.60975676T= GRCh38
NC_000014.8:g.61442394T= , CM000676.1:g.61442394T= GRCh37
NC_000014.7:g.60512147T= NCBI36
NG_053119.1:g.11015A=

Transcript Alleles

HGVS Amino-acid change
ENST00000261249.7:c.1243A= MANE Select ENSP00000261249.6:p.Ile415=
ENST00000261249.6:c.1243A= ENSP00000261249.6:p.Ile415=
NM_020810.3:c.1243A= MANE Select NP_065861.3:p.Ile415=
XM_005267916.2:c.1327A= XP_005267973.2:p.Ile443=
XM_011537017.1:c.1324A= XP_011535319.1:p.Ile442=
NM_001350253.1:c.1327A= NP_001337182.1:p.Ile443=
NM_001350254.1:c.1324A= NP_001337183.1:p.Ile442=