Canonical Allele Identifier: CA486956995
Gene: TRMT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.61442395G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.60975677G>A , CM000676.2:g.60975677G>A GRCh38
NC_000014.8:g.61442395G>A , CM000676.1:g.61442395G>A GRCh37
NC_000014.7:g.60512148G>A NCBI36
NG_053119.1:g.11014C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261249.7:c.1242C>T MANE Select ENSP00000261249.6:p.Pro414=
ENST00000261249.6:c.1242C>T ENSP00000261249.6:p.Pro414=
NM_020810.3:c.1242C>T MANE Select NP_065861.3:p.Pro414=
XM_005267916.2:c.1326C>T XP_005267973.2:p.Pro442=
XM_011537017.1:c.1323C>T XP_011535319.1:p.Pro441=
NM_001350253.1:c.1326C>T NP_001337182.1:p.Pro442=
NM_001350254.1:c.1323C>T NP_001337183.1:p.Pro441=