Canonical Allele Identifier: CA345375048

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237016272A>G (hg19) ; chr1:g.236852972A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852972A>G , CM000663.2:g.236852972A>G	GRCh38
NC_000001.10:g.237016272A>G , CM000663.1:g.237016272A>G	GRCh37
NC_000001.9:g.235082895A>G	NCBI36
NG_008959.1:g.62692A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1837A>G MANE Select	ENSP00000355536.5:p.Asn613Asp
ENST00000535889.6:c.1837A>G	ENSP00000441845.1:p.Asn613Asp
ENST00000650888.1:c.*879A>G	ENSP00000498393.1:n.*879A>G
ENST00000651455.1:c.*581A>G	ENSP00000498963.1:n.*581A>G
ENST00000674797.2:c.1489A>G	ENSP00000502299.2:p.Asn497Asp
ENST00000679569.1:n.2151A>G
ENST00000679842.1:c.1837A>G	ENSP00000506109.1:p.Asn613Asp
ENST00000680454.1:n.2281A>G
ENST00000681102.1:c.1657A>G	ENSP00000505600.1:p.Asn553Asp
ENST00000681177.1:c.1516-6861A>G	ENSP00000506327.1:n.1516-6861A>G
ENST00000681937.1:n.2148-6861A>G
ENST00000366576.3:c.499A>G	ENSP00000355535.3:p.Asn167Asp
ENST00000366577.9:c.1837A>G	ENSP00000355536.5:p.Asn613Asp
ENST00000463959.1:n.1856A>G
ENST00000535889.5:c.1837A>G	ENSP00000441845.1:p.Asn613Asp
NM_000254.2:c.1837A>G	NP_000245.2:p.Asn613Asp
NM_001291939.1:c.1837A>G	NP_001278868.1:p.Asn613Asp
NM_001291940.1:c.616A>G	NP_001278869.1:p.Asn206Asp
XM_005273141.3:c.1834A>G	XP_005273198.1:p.Asn612Asp
XM_006711769.2:c.1837A>G	XP_006711832.1:p.Asn613Asp
XM_006711770.1:c.901A>G	XP_006711833.1:p.Asn301Asp
XM_011544193.1:c.1837A>G	XP_011542495.1:p.Asn613Asp
XM_011544194.1:c.2005A>G	XP_011542496.1:p.Asn669Asp
XM_005273141.5:c.1834A>G	XP_005273198.1:p.Asn612Asp
XM_006711770.3:c.901A>G	XP_006711833.1:p.Asn301Asp
XM_011544194.3:c.2005A>G	XP_011542496.1:p.Asn669Asp
XM_017001329.2:c.2005A>G	XP_016856818.1:p.Asn669Asp
XM_017001330.2:c.2005A>G	XP_016856819.1:p.Asn669Asp
NM_001291940.2:c.616A>G	NP_001278869.1:p.Asn206Asp
NM_000254.3:c.1837A>G MANE Select	NP_000245.2:p.Asn613Asp