Canonical Allele Identifier: CA345374700

Gene: MTR

Linked Data

• gnomAD v4: 1-236852552-G-T
• MyVariant Identifiers: chr1:g.237015852G>T (hg19) ; chr1:g.236852552G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852552G>T , CM000663.2:g.236852552G>T	GRCh38
NC_000001.10:g.237015852G>T , CM000663.1:g.237015852G>T	GRCh37
NC_000001.9:g.235082475G>T	NCBI36
NG_008959.1:g.62272G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1727G>T MANE Select	ENSP00000355536.5:p.Gly576Val
ENST00000535889.6:c.1727G>T	ENSP00000441845.1:p.Gly576Val
ENST00000650888.1:c.*769G>T	ENSP00000498393.1:n.*769G>T
ENST00000651455.1:c.*471G>T	ENSP00000498963.1:n.*471G>T
ENST00000674797.2:c.1379G>T	ENSP00000502299.2:p.Gly460Val
ENST00000679569.1:n.2041G>T
ENST00000679842.1:c.1727G>T	ENSP00000506109.1:p.Gly576Val
ENST00000680454.1:n.2171G>T
ENST00000681102.1:c.1547G>T	ENSP00000505600.1:p.Gly516Val
ENST00000681177.1:c.1516-7281G>T	ENSP00000506327.1:n.1516-7281G>T
ENST00000681937.1:n.2148-7281G>T
ENST00000366576.3:c.389G>T	ENSP00000355535.3:p.Gly130Val
ENST00000366577.9:c.1727G>T	ENSP00000355536.5:p.Gly576Val
ENST00000463959.1:n.1746G>T
ENST00000535889.5:c.1727G>T	ENSP00000441845.1:p.Gly576Val
NM_000254.2:c.1727G>T	NP_000245.2:p.Gly576Val
NM_001291939.1:c.1727G>T	NP_001278868.1:p.Gly576Val
NM_001291940.1:c.506G>T	NP_001278869.1:p.Gly169Val
XM_005273141.3:c.1724G>T	XP_005273198.1:p.Gly575Val
XM_006711769.2:c.1727G>T	XP_006711832.1:p.Gly576Val
XM_006711770.1:c.791G>T	XP_006711833.1:p.Gly264Val
XM_011544193.1:c.1727G>T	XP_011542495.1:p.Gly576Val
XM_011544194.1:c.1895G>T	XP_011542496.1:p.Gly632Val
XM_005273141.5:c.1724G>T	XP_005273198.1:p.Gly575Val
XM_006711770.3:c.791G>T	XP_006711833.1:p.Gly264Val
XM_011544194.3:c.1895G>T	XP_011542496.1:p.Gly632Val
XM_017001329.2:c.1895G>T	XP_016856818.1:p.Gly632Val
XM_017001330.2:c.1895G>T	XP_016856819.1:p.Gly632Val
NM_001291940.2:c.506G>T	NP_001278869.1:p.Gly169Val
NM_000254.3:c.1727G>T MANE Select	NP_000245.2:p.Gly576Val