Canonical Allele Identifier: CA345374970

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237015933T>A (hg19) ; chr1:g.236852633T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852633T>A , CM000663.2:g.236852633T>A	GRCh38
NC_000001.10:g.237015933T>A , CM000663.1:g.237015933T>A	GRCh37
NC_000001.9:g.235082556T>A	NCBI36
NG_008959.1:g.62353T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1808T>A MANE Select	ENSP00000355536.5:p.Ile603Asn
ENST00000535889.6:c.1808T>A	ENSP00000441845.1:p.Ile603Asn
ENST00000650888.1:c.*850T>A	ENSP00000498393.1:n.*850T>A
ENST00000651455.1:c.*552T>A	ENSP00000498963.1:n.*552T>A
ENST00000674797.2:c.1460T>A	ENSP00000502299.2:p.Ile487Asn
ENST00000679569.1:n.2122T>A
ENST00000679842.1:c.1808T>A	ENSP00000506109.1:p.Ile603Asn
ENST00000680454.1:n.2252T>A
ENST00000681102.1:c.1628T>A	ENSP00000505600.1:p.Ile543Asn
ENST00000681177.1:c.1516-7200T>A	ENSP00000506327.1:n.1516-7200T>A
ENST00000681937.1:n.2148-7200T>A
ENST00000366576.3:c.470T>A	ENSP00000355535.3:p.Ile157Asn
ENST00000366577.9:c.1808T>A	ENSP00000355536.5:p.Ile603Asn
ENST00000463959.1:n.1827T>A
ENST00000535889.5:c.1808T>A	ENSP00000441845.1:p.Ile603Asn
NM_000254.2:c.1808T>A	NP_000245.2:p.Ile603Asn
NM_001291939.1:c.1808T>A	NP_001278868.1:p.Ile603Asn
NM_001291940.1:c.587T>A	NP_001278869.1:p.Ile196Asn
XM_005273141.3:c.1805T>A	XP_005273198.1:p.Ile602Asn
XM_006711769.2:c.1808T>A	XP_006711832.1:p.Ile603Asn
XM_006711770.1:c.872T>A	XP_006711833.1:p.Ile291Asn
XM_011544193.1:c.1808T>A	XP_011542495.1:p.Ile603Asn
XM_011544194.1:c.1976T>A	XP_011542496.1:p.Ile659Asn
XM_005273141.5:c.1805T>A	XP_005273198.1:p.Ile602Asn
XM_006711770.3:c.872T>A	XP_006711833.1:p.Ile291Asn
XM_011544194.3:c.1976T>A	XP_011542496.1:p.Ile659Asn
XM_017001329.2:c.1976T>A	XP_016856818.1:p.Ile659Asn
XM_017001330.2:c.1976T>A	XP_016856819.1:p.Ile659Asn
NM_001291940.2:c.587T>A	NP_001278869.1:p.Ile196Asn
NM_000254.3:c.1808T>A MANE Select	NP_000245.2:p.Ile603Asn