Canonical Allele Identifier: CA1661594026

Gene: TRMT11

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.126010399C= , CM000668.2:g.126010399C=	GRCh38
NC_000006.11:g.126331545C= , CM000668.1:g.126331545C=	GRCh37
NC_000006.10:g.126373238C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000334379.11:c.761-854C= MANE Select	ENSP00000333934.5:n.761-854C=
ENST00000648977.1:c.*270-526C=	ENSP00000496820.1:n.*270-526C=
ENST00000334379.9:c.761-854C=	ENSP00000333934.5:n.761-854C=
ENST00000368332.7:c.761-854C=	ENSP00000357316.3:n.761-854C=
ENST00000453993.2:c.156-854C=
ENST00000466316.1:c.195-854C=
ENST00000468097.5:c.*270-854C=	ENSP00000467035.1:n.*270-854C=
ENST00000479748.5:c.*176-854C=	ENSP00000433724.1:n.*176-854C=
NM_001031712.2:c.761-854C=	NP_001026882.2:n.761-854C=
XM_006715546.2:c.761-526C=	XP_006715609.1:n.761-526C=
XR_942548.1:n.959-854C=
XR_942549.1:n.959-526C=
XR_942550.1:n.1059-854C=
NM_001350580.1:c.725-854C=	NP_001337509.1:n.725-854C=
NM_001350581.1:c.572-854C=	NP_001337510.1:n.572-854C=
NM_001350582.1:c.572-854C=	NP_001337511.1:n.572-854C=
NM_001350583.1:c.572-854C=	NP_001337512.1:n.572-854C=
NM_001350584.1:c.572-854C=	NP_001337513.1:n.572-854C=
NM_001350585.1:c.167-854C=	NP_001337514.1:n.167-854C=
NM_001350586.1:c.-267-526C=	NP_001337515.1:n.-267-526C=
NM_001350587.1:c.-267-526C=	NP_001337516.1:n.-267-526C=
NM_001350588.1:c.-267-526C=	NP_001337517.1:n.-267-526C=
NM_001350589.1:c.-267-526C=	NP_001337518.1:n.-267-526C=
NM_001350590.1:c.-508C=	NP_001337519.1:n.-508C=
NM_001350591.1:c.-267-526C=	NP_001337520.1:n.-267-526C=
NM_001350592.1:c.-267-526C=	NP_001337521.1:n.-267-526C=
NM_001350593.1:c.-508C=	NP_001337522.1:n.-508C=
NM_001350594.1:c.-267-526C=	NP_001337523.1:n.-267-526C=
NM_001350595.1:c.-267-526C=	NP_001337524.1:n.-267-526C=
NM_001350596.1:c.-267-526C=	NP_001337525.1:n.-267-526C=
NM_001350597.1:c.-267-526C=	NP_001337526.1:n.-267-526C=
NR_146795.1:n.1071-854C=
NR_146796.1:n.995-854C=
NR_146797.1:n.995-526C=
NR_146798.1:n.971-854C=
NR_146799.1:n.882-854C=
NR_146800.1:n.992-854C=
NR_146801.1:n.1084-854C=
NR_146802.1:n.1226-854C=
NR_146803.1:n.971-526C=
NR_146804.1:n.882-526C=
XM_017011168.1:c.167-854C=	XP_016866657.1:n.167-854C=
XM_024446516.1:c.-508C=	XP_024302284.1:n.-508C=
XR_002956294.1:n.2601C=
NM_001031712.3:c.761-854C= MANE Select	NP_001026882.2:n.761-854C=
NR_146803.2:n.861-526C=
NR_146804.2:n.772-526C=
NM_001350580.2:c.725-854C=	NP_001337509.1:n.725-854C=
NM_001350581.2:c.572-854C=	NP_001337510.1:n.572-854C=
NM_001350582.2:c.572-854C=	NP_001337511.1:n.572-854C=
NM_001350583.2:c.572-854C=	NP_001337512.1:n.572-854C=
NM_001350584.2:c.572-854C=	NP_001337513.1:n.572-854C=
NM_001350585.2:c.167-854C=	NP_001337514.1:n.167-854C=
NM_001350586.2:c.-267-526C=	NP_001337515.1:n.-267-526C=
NM_001350587.2:c.-267-526C=	NP_001337516.1:n.-267-526C=
NM_001350588.2:c.-267-526C=	NP_001337517.1:n.-267-526C=
NM_001350589.2:c.-267-526C=	NP_001337518.1:n.-267-526C=
NM_001350590.2:c.-508C=	NP_001337519.1:n.-508C=
NM_001350591.2:c.-267-526C=	NP_001337520.1:n.-267-526C=
NM_001350592.2:c.-267-526C=	NP_001337521.1:n.-267-526C=
NM_001350593.2:c.-508C=	NP_001337522.1:n.-508C=
NM_001350594.2:c.-267-526C=	NP_001337523.1:n.-267-526C=
NM_001350595.2:c.-267-526C=	NP_001337524.1:n.-267-526C=
NM_001350596.2:c.-267-526C=	NP_001337525.1:n.-267-526C=
NM_001350597.2:c.-267-526C=	NP_001337526.1:n.-267-526C=
NR_146795.2:n.961-854C=
NR_146796.2:n.885-854C=
NR_146797.2:n.885-526C=
NR_146798.2:n.861-854C=
NR_146799.2:n.772-854C=
NR_146800.2:n.882-854C=
NR_146801.2:n.974-854C=
NR_146802.2:n.1116-854C=