Canonical Allele Identifier: CA423816451

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048513T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885213T>A , CM000663.2:g.236885213T>A	GRCh38
NC_000001.10:g.237048513T>A , CM000663.1:g.237048513T>A	GRCh37
NC_000001.9:g.235115136T>A	NCBI36
NG_008959.1:g.94933T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2769T>A MANE Select	ENSP00000355536.5:p.Ser923=
ENST00000535889.6:c.2616T>A	ENSP00000441845.1:p.Ser872=
ENST00000650888.1:c.*1811T>A	ENSP00000498393.1:n.*1811T>A
ENST00000651455.1:c.*1513T>A	ENSP00000498963.1:n.*1513T>A
ENST00000674797.2:c.2421T>A	ENSP00000502299.2:p.Ser807=
ENST00000679569.1:n.3083T>A
ENST00000679842.1:c.2580T>A	ENSP00000506109.1:p.Ser860=
ENST00000680454.1:n.3213T>A
ENST00000681102.1:c.2589T>A	ENSP00000505600.1:p.Ser863=
ENST00000681177.1:c.2331T>A	ENSP00000506327.1:p.Ser777=
ENST00000681937.1:n.2963T>A
ENST00000366576.3:c.1431T>A	ENSP00000355535.3:p.Ser477=
ENST00000366577.9:c.2769T>A	ENSP00000355536.5:p.Ser923=
ENST00000535889.5:c.2616T>A	ENSP00000441845.1:p.Ser872=
NM_000254.2:c.2769T>A	NP_000245.2:p.Ser923=
NM_001291939.1:c.2616T>A	NP_001278868.1:p.Ser872=
NM_001291940.1:c.1548T>A	NP_001278869.1:p.Ser516=
XM_005273141.3:c.2766T>A	XP_005273198.1:p.Ser922=
XM_006711769.2:c.2769T>A	XP_006711832.1:p.Ser923=
XM_006711770.1:c.1833T>A	XP_006711833.1:p.Ser611=
XM_011544193.1:c.2580T>A	XP_011542495.1:p.Ser860=
XM_011544194.1:c.2937T>A	XP_011542496.1:p.Ser979=
XM_005273141.5:c.2766T>A	XP_005273198.1:p.Ser922=
XM_006711770.3:c.1833T>A	XP_006711833.1:p.Ser611=
XM_011544194.3:c.2937T>A	XP_011542496.1:p.Ser979=
XM_017001329.2:c.2784T>A	XP_016856818.1:p.Ser928=
XM_017001330.2:c.2748T>A	XP_016856819.1:p.Ser916=
NM_001291940.2:c.1548T>A	NP_001278869.1:p.Ser516=
NM_000254.3:c.2769T>A MANE Select	NP_000245.2:p.Ser923=