Canonical Allele Identifier: CA345384644

Gene: MTR

Linked Data

• MyVariant Identifiers: chr1:g.237048505T>A (hg19) ; chr1:g.236885205T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885205T>A , CM000663.2:g.236885205T>A	GRCh38
NC_000001.10:g.237048505T>A , CM000663.1:g.237048505T>A	GRCh37
NC_000001.9:g.235115128T>A	NCBI36
NG_008959.1:g.94925T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2761T>A MANE Select	ENSP00000355536.5:p.Tyr921Asn
ENST00000535889.6:c.2608T>A	ENSP00000441845.1:p.Tyr870Asn
ENST00000650888.1:c.*1803T>A	ENSP00000498393.1:n.*1803T>A
ENST00000651455.1:c.*1505T>A	ENSP00000498963.1:n.*1505T>A
ENST00000674797.2:c.2413T>A	ENSP00000502299.2:p.Tyr805Asn
ENST00000679569.1:n.3075T>A
ENST00000679842.1:c.2572T>A	ENSP00000506109.1:p.Tyr858Asn
ENST00000680454.1:n.3205T>A
ENST00000681102.1:c.2581T>A	ENSP00000505600.1:p.Tyr861Asn
ENST00000681177.1:c.2323T>A	ENSP00000506327.1:p.Tyr775Asn
ENST00000681937.1:n.2955T>A
ENST00000366576.3:c.1423T>A	ENSP00000355535.3:p.Tyr475Asn
ENST00000366577.9:c.2761T>A	ENSP00000355536.5:p.Tyr921Asn
ENST00000535889.5:c.2608T>A	ENSP00000441845.1:p.Tyr870Asn
NM_000254.2:c.2761T>A	NP_000245.2:p.Tyr921Asn
NM_001291939.1:c.2608T>A	NP_001278868.1:p.Tyr870Asn
NM_001291940.1:c.1540T>A	NP_001278869.1:p.Tyr514Asn
XM_005273141.3:c.2758T>A	XP_005273198.1:p.Tyr920Asn
XM_006711769.2:c.2761T>A	XP_006711832.1:p.Tyr921Asn
XM_006711770.1:c.1825T>A	XP_006711833.1:p.Tyr609Asn
XM_011544193.1:c.2572T>A	XP_011542495.1:p.Tyr858Asn
XM_011544194.1:c.2929T>A	XP_011542496.1:p.Tyr977Asn
XM_005273141.5:c.2758T>A	XP_005273198.1:p.Tyr920Asn
XM_006711770.3:c.1825T>A	XP_006711833.1:p.Tyr609Asn
XM_011544194.3:c.2929T>A	XP_011542496.1:p.Tyr977Asn
XM_017001329.2:c.2776T>A	XP_016856818.1:p.Tyr926Asn
XM_017001330.2:c.2740T>A	XP_016856819.1:p.Tyr914Asn
NM_001291940.2:c.1540T>A	NP_001278869.1:p.Tyr514Asn
NM_000254.3:c.2761T>A MANE Select	NP_000245.2:p.Tyr921Asn