Canonical Allele Identifier: CA423816326

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048432G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885132G>T , CM000663.2:g.236885132G>T	GRCh38
NC_000001.10:g.237048432G>T , CM000663.1:g.237048432G>T	GRCh37
NC_000001.9:g.235115055G>T	NCBI36
NG_008959.1:g.94852G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2688G>T MANE Select	ENSP00000355536.5:p.Leu896=
ENST00000535889.6:c.2535G>T	ENSP00000441845.1:p.Leu845=
ENST00000650888.1:c.*1730G>T	ENSP00000498393.1:n.*1730G>T
ENST00000651455.1:c.*1432G>T	ENSP00000498963.1:n.*1432G>T
ENST00000674797.2:c.2340G>T	ENSP00000502299.2:p.Leu780=
ENST00000679569.1:n.3002G>T
ENST00000679842.1:c.2499G>T	ENSP00000506109.1:p.Leu833=
ENST00000680454.1:n.3132G>T
ENST00000681102.1:c.2508G>T	ENSP00000505600.1:p.Leu836=
ENST00000681177.1:c.2250G>T	ENSP00000506327.1:p.Leu750=
ENST00000681937.1:n.2882G>T
ENST00000366576.3:c.1350G>T	ENSP00000355535.3:p.Leu450=
ENST00000366577.9:c.2688G>T	ENSP00000355536.5:p.Leu896=
ENST00000535889.5:c.2535G>T	ENSP00000441845.1:p.Leu845=
NM_000254.2:c.2688G>T	NP_000245.2:p.Leu896=
NM_001291939.1:c.2535G>T	NP_001278868.1:p.Leu845=
NM_001291940.1:c.1467G>T	NP_001278869.1:p.Leu489=
XM_005273141.3:c.2685G>T	XP_005273198.1:p.Leu895=
XM_006711769.2:c.2688G>T	XP_006711832.1:p.Leu896=
XM_006711770.1:c.1752G>T	XP_006711833.1:p.Leu584=
XM_011544193.1:c.2499G>T	XP_011542495.1:p.Leu833=
XM_011544194.1:c.2856G>T	XP_011542496.1:p.Leu952=
XM_005273141.5:c.2685G>T	XP_005273198.1:p.Leu895=
XM_006711770.3:c.1752G>T	XP_006711833.1:p.Leu584=
XM_011544194.3:c.2856G>T	XP_011542496.1:p.Leu952=
XM_017001329.2:c.2703G>T	XP_016856818.1:p.Leu901=
XM_017001330.2:c.2667G>T	XP_016856819.1:p.Leu889=
NM_001291940.2:c.1467G>T	NP_001278869.1:p.Leu489=
NM_000254.3:c.2688G>T MANE Select	NP_000245.2:p.Leu896=