Canonical Allele Identifier: CA345384689

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048511T>G (hg19) ; chr1:g.236885211T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885211T>G , CM000663.2:g.236885211T>G	GRCh38
NC_000001.10:g.237048511T>G , CM000663.1:g.237048511T>G	GRCh37
NC_000001.9:g.235115134T>G	NCBI36
NG_008959.1:g.94931T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2767T>G MANE Select	ENSP00000355536.5:p.Ser923Ala
ENST00000535889.6:c.2614T>G	ENSP00000441845.1:p.Ser872Ala
ENST00000650888.1:c.*1809T>G	ENSP00000498393.1:n.*1809T>G
ENST00000651455.1:c.*1511T>G	ENSP00000498963.1:n.*1511T>G
ENST00000674797.2:c.2419T>G	ENSP00000502299.2:p.Ser807Ala
ENST00000679569.1:n.3081T>G
ENST00000679842.1:c.2578T>G	ENSP00000506109.1:p.Ser860Ala
ENST00000680454.1:n.3211T>G
ENST00000681102.1:c.2587T>G	ENSP00000505600.1:p.Ser863Ala
ENST00000681177.1:c.2329T>G	ENSP00000506327.1:p.Ser777Ala
ENST00000681937.1:n.2961T>G
ENST00000366576.3:c.1429T>G	ENSP00000355535.3:p.Ser477Ala
ENST00000366577.9:c.2767T>G	ENSP00000355536.5:p.Ser923Ala
ENST00000535889.5:c.2614T>G	ENSP00000441845.1:p.Ser872Ala
NM_000254.2:c.2767T>G	NP_000245.2:p.Ser923Ala
NM_001291939.1:c.2614T>G	NP_001278868.1:p.Ser872Ala
NM_001291940.1:c.1546T>G	NP_001278869.1:p.Ser516Ala
XM_005273141.3:c.2764T>G	XP_005273198.1:p.Ser922Ala
XM_006711769.2:c.2767T>G	XP_006711832.1:p.Ser923Ala
XM_006711770.1:c.1831T>G	XP_006711833.1:p.Ser611Ala
XM_011544193.1:c.2578T>G	XP_011542495.1:p.Ser860Ala
XM_011544194.1:c.2935T>G	XP_011542496.1:p.Ser979Ala
XM_005273141.5:c.2764T>G	XP_005273198.1:p.Ser922Ala
XM_006711770.3:c.1831T>G	XP_006711833.1:p.Ser611Ala
XM_011544194.3:c.2935T>G	XP_011542496.1:p.Ser979Ala
XM_017001329.2:c.2782T>G	XP_016856818.1:p.Ser928Ala
XM_017001330.2:c.2746T>G	XP_016856819.1:p.Ser916Ala
NM_001291940.2:c.1546T>G	NP_001278869.1:p.Ser516Ala
NM_000254.3:c.2767T>G MANE Select	NP_000245.2:p.Ser923Ala