Canonical Allele Identifier: CA423816334

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048435A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885135A>G , CM000663.2:g.236885135A>G	GRCh38
NC_000001.10:g.237048435A>G , CM000663.1:g.237048435A>G	GRCh37
NC_000001.9:g.235115058A>G	NCBI36
NG_008959.1:g.94855A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2691A>G MANE Select	ENSP00000355536.5:p.Leu897=
ENST00000535889.6:c.2538A>G	ENSP00000441845.1:p.Leu846=
ENST00000650888.1:c.*1733A>G	ENSP00000498393.1:n.*1733A>G
ENST00000651455.1:c.*1435A>G	ENSP00000498963.1:n.*1435A>G
ENST00000674797.2:c.2343A>G	ENSP00000502299.2:p.Leu781=
ENST00000679569.1:n.3005A>G
ENST00000679842.1:c.2502A>G	ENSP00000506109.1:p.Leu834=
ENST00000680454.1:n.3135A>G
ENST00000681102.1:c.2511A>G	ENSP00000505600.1:p.Leu837=
ENST00000681177.1:c.2253A>G	ENSP00000506327.1:p.Leu751=
ENST00000681937.1:n.2885A>G
ENST00000366576.3:c.1353A>G	ENSP00000355535.3:p.Leu451=
ENST00000366577.9:c.2691A>G	ENSP00000355536.5:p.Leu897=
ENST00000535889.5:c.2538A>G	ENSP00000441845.1:p.Leu846=
NM_000254.2:c.2691A>G	NP_000245.2:p.Leu897=
NM_001291939.1:c.2538A>G	NP_001278868.1:p.Leu846=
NM_001291940.1:c.1470A>G	NP_001278869.1:p.Leu490=
XM_005273141.3:c.2688A>G	XP_005273198.1:p.Leu896=
XM_006711769.2:c.2691A>G	XP_006711832.1:p.Leu897=
XM_006711770.1:c.1755A>G	XP_006711833.1:p.Leu585=
XM_011544193.1:c.2502A>G	XP_011542495.1:p.Leu834=
XM_011544194.1:c.2859A>G	XP_011542496.1:p.Leu953=
XM_005273141.5:c.2688A>G	XP_005273198.1:p.Leu896=
XM_006711770.3:c.1755A>G	XP_006711833.1:p.Leu585=
XM_011544194.3:c.2859A>G	XP_011542496.1:p.Leu953=
XM_017001329.2:c.2706A>G	XP_016856818.1:p.Leu902=
XM_017001330.2:c.2670A>G	XP_016856819.1:p.Leu890=
NM_001291940.2:c.1470A>G	NP_001278869.1:p.Leu490=
NM_000254.3:c.2691A>G MANE Select	NP_000245.2:p.Leu897=