Canonical Allele Identifier: CA345374908

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237015906T>G (hg19) ; chr1:g.236852606T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852606T>G , CM000663.2:g.236852606T>G	GRCh38
NC_000001.10:g.237015906T>G , CM000663.1:g.237015906T>G	GRCh37
NC_000001.9:g.235082529T>G	NCBI36
NG_008959.1:g.62326T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1781T>G MANE Select	ENSP00000355536.5:p.Met594Arg
ENST00000535889.6:c.1781T>G	ENSP00000441845.1:p.Met594Arg
ENST00000650888.1:c.*823T>G	ENSP00000498393.1:n.*823T>G
ENST00000651455.1:c.*525T>G	ENSP00000498963.1:n.*525T>G
ENST00000674797.2:c.1433T>G	ENSP00000502299.2:p.Met478Arg
ENST00000679569.1:n.2095T>G
ENST00000679842.1:c.1781T>G	ENSP00000506109.1:p.Met594Arg
ENST00000680454.1:n.2225T>G
ENST00000681102.1:c.1601T>G	ENSP00000505600.1:p.Met534Arg
ENST00000681177.1:c.1516-7227T>G	ENSP00000506327.1:n.1516-7227T>G
ENST00000681937.1:n.2148-7227T>G
ENST00000366576.3:c.443T>G	ENSP00000355535.3:p.Met148Arg
ENST00000366577.9:c.1781T>G	ENSP00000355536.5:p.Met594Arg
ENST00000463959.1:n.1800T>G
ENST00000535889.5:c.1781T>G	ENSP00000441845.1:p.Met594Arg
NM_000254.2:c.1781T>G	NP_000245.2:p.Met594Arg
NM_001291939.1:c.1781T>G	NP_001278868.1:p.Met594Arg
NM_001291940.1:c.560T>G	NP_001278869.1:p.Met187Arg
XM_005273141.3:c.1778T>G	XP_005273198.1:p.Met593Arg
XM_006711769.2:c.1781T>G	XP_006711832.1:p.Met594Arg
XM_006711770.1:c.845T>G	XP_006711833.1:p.Met282Arg
XM_011544193.1:c.1781T>G	XP_011542495.1:p.Met594Arg
XM_011544194.1:c.1949T>G	XP_011542496.1:p.Met650Arg
XM_005273141.5:c.1778T>G	XP_005273198.1:p.Met593Arg
XM_006711770.3:c.845T>G	XP_006711833.1:p.Met282Arg
XM_011544194.3:c.1949T>G	XP_011542496.1:p.Met650Arg
XM_017001329.2:c.1949T>G	XP_016856818.1:p.Met650Arg
XM_017001330.2:c.1949T>G	XP_016856819.1:p.Met650Arg
NM_001291940.2:c.560T>G	NP_001278869.1:p.Met187Arg
NM_000254.3:c.1781T>G MANE Select	NP_000245.2:p.Met594Arg