Canonical Allele Identifier: CA345383287

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237044129T>G (hg19) ; chr1:g.236880829T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236880829T>G , CM000663.2:g.236880829T>G	GRCh38
NC_000001.10:g.237044129T>G , CM000663.1:g.237044129T>G	GRCh37
NC_000001.9:g.235110752T>G	NCBI36
NG_008959.1:g.90549T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2669T>G MANE Select	ENSP00000355536.5:p.Val890Gly
ENST00000535889.6:c.2516T>G	ENSP00000441845.1:p.Val839Gly
ENST00000650888.1:c.*1711T>G	ENSP00000498393.1:n.*1711T>G
ENST00000651455.1:c.*1413T>G	ENSP00000498963.1:n.*1413T>G
ENST00000674797.2:c.2321T>G	ENSP00000502299.2:p.Val774Gly
ENST00000679569.1:n.2983T>G
ENST00000679842.1:c.2480T>G	ENSP00000506109.1:p.Val827Gly
ENST00000680454.1:n.3113T>G
ENST00000681102.1:c.2489T>G	ENSP00000505600.1:p.Val830Gly
ENST00000681177.1:c.2231T>G	ENSP00000506327.1:p.Val744Gly
ENST00000681937.1:n.2863T>G
ENST00000366576.3:c.1331T>G	ENSP00000355535.3:p.Val444Gly
ENST00000366577.9:c.2669T>G	ENSP00000355536.5:p.Val890Gly
ENST00000535889.5:c.2516T>G	ENSP00000441845.1:p.Val839Gly
NM_000254.2:c.2669T>G	NP_000245.2:p.Val890Gly
NM_001291939.1:c.2516T>G	NP_001278868.1:p.Val839Gly
NM_001291940.1:c.1448T>G	NP_001278869.1:p.Val483Gly
XM_005273141.3:c.2666T>G	XP_005273198.1:p.Val889Gly
XM_006711769.2:c.2669T>G	XP_006711832.1:p.Val890Gly
XM_006711770.1:c.1733T>G	XP_006711833.1:p.Val578Gly
XM_011544193.1:c.2480T>G	XP_011542495.1:p.Val827Gly
XM_011544194.1:c.2837T>G	XP_011542496.1:p.Val946Gly
XM_005273141.5:c.2666T>G	XP_005273198.1:p.Val889Gly
XM_006711770.3:c.1733T>G	XP_006711833.1:p.Val578Gly
XM_011544194.3:c.2837T>G	XP_011542496.1:p.Val946Gly
XM_017001329.2:c.2684T>G	XP_016856818.1:p.Val895Gly
XM_017001330.2:c.2648T>G	XP_016856819.1:p.Val883Gly
NM_001291940.2:c.1448T>G	NP_001278869.1:p.Val483Gly
NM_000254.3:c.2669T>G MANE Select	NP_000245.2:p.Val890Gly