Canonical Allele Identifier: CA423811490

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237015892C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852592C>A , CM000663.2:g.236852592C>A	GRCh38
NC_000001.10:g.237015892C>A , CM000663.1:g.237015892C>A	GRCh37
NC_000001.9:g.235082515C>A	NCBI36
NG_008959.1:g.62312C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.1767C>A MANE Select	ENSP00000355536.5:p.Ala589=
ENST00000535889.6:c.1767C>A	ENSP00000441845.1:p.Ala589=
ENST00000650888.1:c.*809C>A	ENSP00000498393.1:n.*809C>A
ENST00000651455.1:c.*511C>A	ENSP00000498963.1:n.*511C>A
ENST00000674797.2:c.1419C>A	ENSP00000502299.2:p.Ala473=
ENST00000679569.1:n.2081C>A
ENST00000679842.1:c.1767C>A	ENSP00000506109.1:p.Ala589=
ENST00000680454.1:n.2211C>A
ENST00000681102.1:c.1587C>A	ENSP00000505600.1:p.Ala529=
ENST00000681177.1:c.1516-7241C>A	ENSP00000506327.1:n.1516-7241C>A
ENST00000681937.1:n.2148-7241C>A
ENST00000366576.3:c.429C>A	ENSP00000355535.3:p.Ala143=
ENST00000366577.9:c.1767C>A	ENSP00000355536.5:p.Ala589=
ENST00000463959.1:n.1786C>A
ENST00000535889.5:c.1767C>A	ENSP00000441845.1:p.Ala589=
NM_000254.2:c.1767C>A	NP_000245.2:p.Ala589=
NM_001291939.1:c.1767C>A	NP_001278868.1:p.Ala589=
NM_001291940.1:c.546C>A	NP_001278869.1:p.Ala182=
XM_005273141.3:c.1764C>A	XP_005273198.1:p.Ala588=
XM_006711769.2:c.1767C>A	XP_006711832.1:p.Ala589=
XM_006711770.1:c.831C>A	XP_006711833.1:p.Ala277=
XM_011544193.1:c.1767C>A	XP_011542495.1:p.Ala589=
XM_011544194.1:c.1935C>A	XP_011542496.1:p.Ala645=
XM_005273141.5:c.1764C>A	XP_005273198.1:p.Ala588=
XM_006711770.3:c.831C>A	XP_006711833.1:p.Ala277=
XM_011544194.3:c.1935C>A	XP_011542496.1:p.Ala645=
XM_017001329.2:c.1935C>A	XP_016856818.1:p.Ala645=
XM_017001330.2:c.1935C>A	XP_016856819.1:p.Ala645=
NM_001291940.2:c.546C>A	NP_001278869.1:p.Ala182=
NM_000254.3:c.1767C>A MANE Select	NP_000245.2:p.Ala589=