Canonical Allele Identifier: CA423811736

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237016253C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852953C>G , CM000663.2:g.236852953C>G	GRCh38
NC_000001.10:g.237016253C>G , CM000663.1:g.237016253C>G	GRCh37
NC_000001.9:g.235082876C>G	NCBI36
NG_008959.1:g.62673C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1818C>G MANE Select	ENSP00000355536.5:p.Gly606=
ENST00000535889.6:c.1818C>G	ENSP00000441845.1:p.Gly606=
ENST00000650888.1:c.*860C>G	ENSP00000498393.1:n.*860C>G
ENST00000651455.1:c.*562C>G	ENSP00000498963.1:n.*562C>G
ENST00000674797.2:c.1470C>G	ENSP00000502299.2:p.Gly490=
ENST00000679569.1:n.2132C>G
ENST00000679842.1:c.1818C>G	ENSP00000506109.1:p.Gly606=
ENST00000680454.1:n.2262C>G
ENST00000681102.1:c.1638C>G	ENSP00000505600.1:p.Gly546=
ENST00000681177.1:c.1516-6880C>G	ENSP00000506327.1:n.1516-6880C>G
ENST00000681937.1:n.2148-6880C>G
ENST00000366576.3:c.480C>G	ENSP00000355535.3:p.Gly160=
ENST00000366577.9:c.1818C>G	ENSP00000355536.5:p.Gly606=
ENST00000463959.1:n.1837C>G
ENST00000535889.5:c.1818C>G	ENSP00000441845.1:p.Gly606=
NM_000254.2:c.1818C>G	NP_000245.2:p.Gly606=
NM_001291939.1:c.1818C>G	NP_001278868.1:p.Gly606=
NM_001291940.1:c.597C>G	NP_001278869.1:p.Gly199=
XM_005273141.3:c.1815C>G	XP_005273198.1:p.Gly605=
XM_006711769.2:c.1818C>G	XP_006711832.1:p.Gly606=
XM_006711770.1:c.882C>G	XP_006711833.1:p.Gly294=
XM_011544193.1:c.1818C>G	XP_011542495.1:p.Gly606=
XM_011544194.1:c.1986C>G	XP_011542496.1:p.Gly662=
XM_005273141.5:c.1815C>G	XP_005273198.1:p.Gly605=
XM_006711770.3:c.882C>G	XP_006711833.1:p.Gly294=
XM_011544194.3:c.1986C>G	XP_011542496.1:p.Gly662=
XM_017001329.2:c.1986C>G	XP_016856818.1:p.Gly662=
XM_017001330.2:c.1986C>G	XP_016856819.1:p.Gly662=
NM_001291940.2:c.597C>G	NP_001278869.1:p.Gly199=
NM_000254.3:c.1818C>G MANE Select	NP_000245.2:p.Gly606=