Canonical Allele Identifier: CA345374716

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237015857T>G (hg19) ; chr1:g.236852557T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852557T>G , CM000663.2:g.236852557T>G	GRCh38
NC_000001.10:g.237015857T>G , CM000663.1:g.237015857T>G	GRCh37
NC_000001.9:g.235082480T>G	NCBI36
NG_008959.1:g.62277T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1732T>G MANE Select	ENSP00000355536.5:p.Ser578Ala
ENST00000535889.6:c.1732T>G	ENSP00000441845.1:p.Ser578Ala
ENST00000650888.1:c.*774T>G	ENSP00000498393.1:n.*774T>G
ENST00000651455.1:c.*476T>G	ENSP00000498963.1:n.*476T>G
ENST00000674797.2:c.1384T>G	ENSP00000502299.2:p.Ser462Ala
ENST00000679569.1:n.2046T>G
ENST00000679842.1:c.1732T>G	ENSP00000506109.1:p.Ser578Ala
ENST00000680454.1:n.2176T>G
ENST00000681102.1:c.1552T>G	ENSP00000505600.1:p.Ser518Ala
ENST00000681177.1:c.1516-7276T>G	ENSP00000506327.1:n.1516-7276T>G
ENST00000681937.1:n.2148-7276T>G
ENST00000366576.3:c.394T>G	ENSP00000355535.3:p.Ser132Ala
ENST00000366577.9:c.1732T>G	ENSP00000355536.5:p.Ser578Ala
ENST00000463959.1:n.1751T>G
ENST00000535889.5:c.1732T>G	ENSP00000441845.1:p.Ser578Ala
NM_000254.2:c.1732T>G	NP_000245.2:p.Ser578Ala
NM_001291939.1:c.1732T>G	NP_001278868.1:p.Ser578Ala
NM_001291940.1:c.511T>G	NP_001278869.1:p.Ser171Ala
XM_005273141.3:c.1729T>G	XP_005273198.1:p.Ser577Ala
XM_006711769.2:c.1732T>G	XP_006711832.1:p.Ser578Ala
XM_006711770.1:c.796T>G	XP_006711833.1:p.Ser266Ala
XM_011544193.1:c.1732T>G	XP_011542495.1:p.Ser578Ala
XM_011544194.1:c.1900T>G	XP_011542496.1:p.Ser634Ala
XM_005273141.5:c.1729T>G	XP_005273198.1:p.Ser577Ala
XM_006711770.3:c.796T>G	XP_006711833.1:p.Ser266Ala
XM_011544194.3:c.1900T>G	XP_011542496.1:p.Ser634Ala
XM_017001329.2:c.1900T>G	XP_016856818.1:p.Ser634Ala
XM_017001330.2:c.1900T>G	XP_016856819.1:p.Ser634Ala
NM_001291940.2:c.511T>G	NP_001278869.1:p.Ser171Ala
NM_000254.3:c.1732T>G MANE Select	NP_000245.2:p.Ser578Ala