Canonical Allele Identifier: CA423816812

Gene: MTR

Linked Data

• gnomAD v4: 1-236829240-T-A
• MyVariant Identifiers: chr1:g.236992540T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236829240T>A , CM000663.2:g.236829240T>A	GRCh38
NC_000001.10:g.236992540T>A , CM000663.1:g.236992540T>A	GRCh37
NC_000001.9:g.235059163T>A	NCBI36
NG_008959.1:g.38960T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1047T>A MANE Select	ENSP00000355536.5:p.Thr349=
ENST00000535889.6:c.1047T>A	ENSP00000441845.1:p.Thr349=
ENST00000650888.1:c.*89T>A	ENSP00000498393.1:n.*89T>A
ENST00000651455.1:c.1047T>A	ENSP00000498963.1:p.Thr349=
ENST00000674797.2:c.699T>A	ENSP00000502299.2:p.Thr233=
ENST00000679569.1:n.1361T>A
ENST00000679842.1:c.1047T>A	ENSP00000506109.1:p.Thr349=
ENST00000680454.1:n.1491T>A
ENST00000681102.1:c.1047T>A	ENSP00000505600.1:p.Thr349=
ENST00000681177.1:c.1047T>A	ENSP00000506327.1:p.Thr349=
ENST00000681937.1:n.1679T>A
ENST00000366577.9:c.1047T>A	ENSP00000355536.5:p.Thr349=
ENST00000463959.1:n.1066T>A
ENST00000535889.5:c.1047T>A	ENSP00000441845.1:p.Thr349=
NM_000254.2:c.1047T>A	NP_000245.2:p.Thr349=
NM_001291939.1:c.1047T>A	NP_001278868.1:p.Thr349=
NM_001291940.1:c.-62T>A	NP_001278869.1:n.-62T>A
XM_005273141.3:c.1044T>A	XP_005273198.1:p.Thr348=
XM_006711769.2:c.1047T>A	XP_006711832.1:p.Thr349=
XM_006711770.1:c.111T>A	XP_006711833.1:p.Thr37=
XM_011544193.1:c.1047T>A	XP_011542495.1:p.Thr349=
XM_011544194.1:c.1215T>A	XP_011542496.1:p.Thr405=
XM_005273141.5:c.1044T>A	XP_005273198.1:p.Thr348=
XM_006711770.3:c.111T>A	XP_006711833.1:p.Thr37=
XM_011544194.3:c.1215T>A	XP_011542496.1:p.Thr405=
XM_017001329.2:c.1215T>A	XP_016856818.1:p.Thr405=
XM_017001330.2:c.1215T>A	XP_016856819.1:p.Thr405=
NM_001291940.2:c.-62T>A	NP_001278869.1:n.-62T>A
NM_000254.3:c.1047T>A MANE Select	NP_000245.2:p.Thr349=