Canonical Allele Identifier: CA423811728

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237016250T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852950T>C , CM000663.2:g.236852950T>C	GRCh38
NC_000001.10:g.237016250T>C , CM000663.1:g.237016250T>C	GRCh37
NC_000001.9:g.235082873T>C	NCBI36
NG_008959.1:g.62670T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1815T>C MANE Select	ENSP00000355536.5:p.Ser605=
ENST00000535889.6:c.1815T>C	ENSP00000441845.1:p.Ser605=
ENST00000650888.1:c.*857T>C	ENSP00000498393.1:n.*857T>C
ENST00000651455.1:c.*559T>C	ENSP00000498963.1:n.*559T>C
ENST00000674797.2:c.1467T>C	ENSP00000502299.2:p.Ser489=
ENST00000679569.1:n.2129T>C
ENST00000679842.1:c.1815T>C	ENSP00000506109.1:p.Ser605=
ENST00000680454.1:n.2259T>C
ENST00000681102.1:c.1635T>C	ENSP00000505600.1:p.Ser545=
ENST00000681177.1:c.1516-6883T>C	ENSP00000506327.1:n.1516-6883T>C
ENST00000681937.1:n.2148-6883T>C
ENST00000366576.3:c.477T>C	ENSP00000355535.3:p.Ser159=
ENST00000366577.9:c.1815T>C	ENSP00000355536.5:p.Ser605=
ENST00000463959.1:n.1834T>C
ENST00000535889.5:c.1815T>C	ENSP00000441845.1:p.Ser605=
NM_000254.2:c.1815T>C	NP_000245.2:p.Ser605=
NM_001291939.1:c.1815T>C	NP_001278868.1:p.Ser605=
NM_001291940.1:c.594T>C	NP_001278869.1:p.Ser198=
XM_005273141.3:c.1812T>C	XP_005273198.1:p.Ser604=
XM_006711769.2:c.1815T>C	XP_006711832.1:p.Ser605=
XM_006711770.1:c.879T>C	XP_006711833.1:p.Ser293=
XM_011544193.1:c.1815T>C	XP_011542495.1:p.Ser605=
XM_011544194.1:c.1983T>C	XP_011542496.1:p.Ser661=
XM_005273141.5:c.1812T>C	XP_005273198.1:p.Ser604=
XM_006711770.3:c.879T>C	XP_006711833.1:p.Ser293=
XM_011544194.3:c.1983T>C	XP_011542496.1:p.Ser661=
XM_017001329.2:c.1983T>C	XP_016856818.1:p.Ser661=
XM_017001330.2:c.1983T>C	XP_016856819.1:p.Ser661=
NM_001291940.2:c.594T>C	NP_001278869.1:p.Ser198=
NM_000254.3:c.1815T>C MANE Select	NP_000245.2:p.Ser605=