Canonical Allele Identifier: CA345374948

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237015923T>G (hg19) ; chr1:g.236852623T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852623T>G , CM000663.2:g.236852623T>G	GRCh38
NC_000001.10:g.237015923T>G , CM000663.1:g.237015923T>G	GRCh37
NC_000001.9:g.235082546T>G	NCBI36
NG_008959.1:g.62343T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1798T>G MANE Select	ENSP00000355536.5:p.Tyr600Asp
ENST00000535889.6:c.1798T>G	ENSP00000441845.1:p.Tyr600Asp
ENST00000650888.1:c.*840T>G	ENSP00000498393.1:n.*840T>G
ENST00000651455.1:c.*542T>G	ENSP00000498963.1:n.*542T>G
ENST00000674797.2:c.1450T>G	ENSP00000502299.2:p.Tyr484Asp
ENST00000679569.1:n.2112T>G
ENST00000679842.1:c.1798T>G	ENSP00000506109.1:p.Tyr600Asp
ENST00000680454.1:n.2242T>G
ENST00000681102.1:c.1618T>G	ENSP00000505600.1:p.Tyr540Asp
ENST00000681177.1:c.1516-7210T>G	ENSP00000506327.1:n.1516-7210T>G
ENST00000681937.1:n.2148-7210T>G
ENST00000366576.3:c.460T>G	ENSP00000355535.3:p.Tyr154Asp
ENST00000366577.9:c.1798T>G	ENSP00000355536.5:p.Tyr600Asp
ENST00000463959.1:n.1817T>G
ENST00000535889.5:c.1798T>G	ENSP00000441845.1:p.Tyr600Asp
NM_000254.2:c.1798T>G	NP_000245.2:p.Tyr600Asp
NM_001291939.1:c.1798T>G	NP_001278868.1:p.Tyr600Asp
NM_001291940.1:c.577T>G	NP_001278869.1:p.Tyr193Asp
XM_005273141.3:c.1795T>G	XP_005273198.1:p.Tyr599Asp
XM_006711769.2:c.1798T>G	XP_006711832.1:p.Tyr600Asp
XM_006711770.1:c.862T>G	XP_006711833.1:p.Tyr288Asp
XM_011544193.1:c.1798T>G	XP_011542495.1:p.Tyr600Asp
XM_011544194.1:c.1966T>G	XP_011542496.1:p.Tyr656Asp
XM_005273141.5:c.1795T>G	XP_005273198.1:p.Tyr599Asp
XM_006711770.3:c.862T>G	XP_006711833.1:p.Tyr288Asp
XM_011544194.3:c.1966T>G	XP_011542496.1:p.Tyr656Asp
XM_017001329.2:c.1966T>G	XP_016856818.1:p.Tyr656Asp
XM_017001330.2:c.1966T>G	XP_016856819.1:p.Tyr656Asp
NM_001291940.2:c.577T>G	NP_001278869.1:p.Tyr193Asp
NM_000254.3:c.1798T>G MANE Select	NP_000245.2:p.Tyr600Asp