Canonical Allele Identifier: CA423816239

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237044136G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236880836G>T , CM000663.2:g.236880836G>T	GRCh38
NC_000001.10:g.237044136G>T , CM000663.1:g.237044136G>T	GRCh37
NC_000001.9:g.235110759G>T	NCBI36
NG_008959.1:g.90556G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2676G>T MANE Select	ENSP00000355536.5:p.Val892=
ENST00000535889.6:c.2523G>T	ENSP00000441845.1:p.Val841=
ENST00000650888.1:c.*1718G>T	ENSP00000498393.1:n.*1718G>T
ENST00000651455.1:c.*1420G>T	ENSP00000498963.1:n.*1420G>T
ENST00000674797.2:c.2328G>T	ENSP00000502299.2:p.Val776=
ENST00000679569.1:n.2990G>T
ENST00000679842.1:c.2487G>T	ENSP00000506109.1:p.Val829=
ENST00000680454.1:n.3120G>T
ENST00000681102.1:c.2496G>T	ENSP00000505600.1:p.Val832=
ENST00000681177.1:c.2238G>T	ENSP00000506327.1:p.Val746=
ENST00000681937.1:n.2870G>T
ENST00000366576.3:c.1338G>T	ENSP00000355535.3:p.Val446=
ENST00000366577.9:c.2676G>T	ENSP00000355536.5:p.Val892=
ENST00000535889.5:c.2523G>T	ENSP00000441845.1:p.Val841=
NM_000254.2:c.2676G>T	NP_000245.2:p.Val892=
NM_001291939.1:c.2523G>T	NP_001278868.1:p.Val841=
NM_001291940.1:c.1455G>T	NP_001278869.1:p.Val485=
XM_005273141.3:c.2673G>T	XP_005273198.1:p.Val891=
XM_006711769.2:c.2676G>T	XP_006711832.1:p.Val892=
XM_006711770.1:c.1740G>T	XP_006711833.1:p.Val580=
XM_011544193.1:c.2487G>T	XP_011542495.1:p.Val829=
XM_011544194.1:c.2844G>T	XP_011542496.1:p.Val948=
XM_005273141.5:c.2673G>T	XP_005273198.1:p.Val891=
XM_006711770.3:c.1740G>T	XP_006711833.1:p.Val580=
XM_011544194.3:c.2844G>T	XP_011542496.1:p.Val948=
XM_017001329.2:c.2691G>T	XP_016856818.1:p.Val897=
XM_017001330.2:c.2655G>T	XP_016856819.1:p.Val885=
NM_001291940.2:c.1455G>T	NP_001278869.1:p.Val485=
NM_000254.3:c.2676G>T MANE Select	NP_000245.2:p.Val892=