Canonical Allele Identifier: CA2830541881

Gene: TRMT11

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.125999731G>T , CM000668.2:g.125999731G>T	GRCh38
NC_000006.11:g.126320877G>T , CM000668.1:g.126320877G>T	GRCh37
NC_000006.10:g.126362570G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334379.11:c.679+118G>T MANE Select	ENSP00000333934.5:n.679+118G>T
ENST00000648977.1:c.679+118G>T	ENSP00000496820.1:n.679+118G>T
ENST00000334379.9:c.679+118G>T	ENSP00000333934.5:n.679+118G>T
ENST00000368332.7:c.679+118G>T	ENSP00000357316.3:n.679+118G>T
ENST00000453993.2:c.74+118G>T
ENST00000461129.5:c.*348+118G>T	ENSP00000467603.1:n.*348+118G>T
ENST00000468097.5:c.679+118G>T	ENSP00000467035.1:n.679+118G>T
ENST00000479748.5:c.679+118G>T	ENSP00000433724.1:n.679+118G>T
NM_001031712.2:c.679+118G>T	NP_001026882.2:n.679+118G>T
XM_006715546.2:c.679+118G>T	XP_006715609.1:n.679+118G>T
XM_011536044.1:c.679+118G>T	XP_011534346.1:n.679+118G>T
XR_942548.1:n.788+118G>T
XR_942549.1:n.788+118G>T
XR_942550.1:n.788+118G>T
NM_001350580.1:c.643+118G>T	NP_001337509.1:n.643+118G>T
NM_001350581.1:c.490+118G>T	NP_001337510.1:n.490+118G>T
NM_001350582.1:c.490+118G>T	NP_001337511.1:n.490+118G>T
NM_001350583.1:c.490+118G>T	NP_001337512.1:n.490+118G>T
NM_001350584.1:c.490+118G>T	NP_001337513.1:n.490+118G>T
NM_001350585.1:c.85+118G>T	NP_001337514.1:n.85+118G>T
NM_001350586.1:c.-349+118G>T	NP_001337515.1:n.-349+118G>T
NM_001350587.1:c.-459+118G>T	NP_001337516.1:n.-459+118G>T
NM_001350588.1:c.-349+118G>T	NP_001337517.1:n.-349+118G>T
NM_001350589.1:c.-551+118G>T	NP_001337518.1:n.-551+118G>T
NM_001350590.1:c.-700+118G>T	NP_001337519.1:n.-700+118G>T
NM_001350591.1:c.-438+118G>T	NP_001337520.1:n.-438+118G>T
NM_001350592.1:c.-462+118G>T	NP_001337521.1:n.-462+118G>T
NM_001350593.1:c.-813+118G>T	NP_001337522.1:n.-813+118G>T
NM_001350594.1:c.-462+118G>T	NP_001337523.1:n.-462+118G>T
NM_001350595.1:c.-462+118G>T	NP_001337524.1:n.-462+118G>T
NM_001350596.1:c.-438+118G>T	NP_001337525.1:n.-438+118G>T
NM_001350597.1:c.-462+118G>T	NP_001337526.1:n.-462+118G>T
NR_146795.1:n.800+118G>T
NR_146796.1:n.800+118G>T
NR_146797.1:n.800+118G>T
NR_146798.1:n.800+118G>T
NR_146799.1:n.800+118G>T
NR_146800.1:n.800+118G>T
NR_146801.1:n.800+118G>T
NR_146802.1:n.800+118G>T
NR_146803.1:n.800+118G>T
NR_146804.1:n.800+118G>T
XM_017011168.1:c.85+118G>T	XP_016866657.1:n.85+118G>T
XM_024446516.1:c.-700+118G>T	XP_024302284.1:n.-700+118G>T
XR_002956294.1:n.777+118G>T
NM_001031712.3:c.679+118G>T MANE Select	NP_001026882.2:n.679+118G>T
NR_146803.2:n.690+118G>T
NR_146804.2:n.690+118G>T
NM_001350580.2:c.643+118G>T	NP_001337509.1:n.643+118G>T
NM_001350581.2:c.490+118G>T	NP_001337510.1:n.490+118G>T
NM_001350582.2:c.490+118G>T	NP_001337511.1:n.490+118G>T
NM_001350583.2:c.490+118G>T	NP_001337512.1:n.490+118G>T
NM_001350584.2:c.490+118G>T	NP_001337513.1:n.490+118G>T
NM_001350585.2:c.85+118G>T	NP_001337514.1:n.85+118G>T
NM_001350586.2:c.-349+118G>T	NP_001337515.1:n.-349+118G>T
NM_001350587.2:c.-459+118G>T	NP_001337516.1:n.-459+118G>T
NM_001350588.2:c.-349+118G>T	NP_001337517.1:n.-349+118G>T
NM_001350589.2:c.-551+118G>T	NP_001337518.1:n.-551+118G>T
NM_001350590.2:c.-700+118G>T	NP_001337519.1:n.-700+118G>T
NM_001350591.2:c.-438+118G>T	NP_001337520.1:n.-438+118G>T
NM_001350592.2:c.-462+118G>T	NP_001337521.1:n.-462+118G>T
NM_001350593.2:c.-813+118G>T	NP_001337522.1:n.-813+118G>T
NM_001350594.2:c.-462+118G>T	NP_001337523.1:n.-462+118G>T
NM_001350595.2:c.-462+118G>T	NP_001337524.1:n.-462+118G>T
NM_001350596.2:c.-438+118G>T	NP_001337525.1:n.-438+118G>T
NM_001350597.2:c.-462+118G>T	NP_001337526.1:n.-462+118G>T
NR_146795.2:n.690+118G>T
NR_146796.2:n.690+118G>T
NR_146797.2:n.690+118G>T
NR_146798.2:n.690+118G>T
NR_146799.2:n.690+118G>T
NR_146800.2:n.690+118G>T
NR_146801.2:n.690+118G>T
NR_146802.2:n.690+118G>T