Canonical Allele Identifier: CA345374974

Gene: MTR

Linked Data

• gnomAD v4: 1-236852635-A-C
• MyVariant Identifiers: chr1:g.237015935A>C (hg19) ; chr1:g.236852635A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852635A>C , CM000663.2:g.236852635A>C	GRCh38
NC_000001.10:g.237015935A>C , CM000663.1:g.237015935A>C	GRCh37
NC_000001.9:g.235082558A>C	NCBI36
NG_008959.1:g.62355A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1810A>C MANE Select	ENSP00000355536.5:p.Lys604Gln
ENST00000535889.6:c.1810A>C	ENSP00000441845.1:p.Lys604Gln
ENST00000650888.1:c.*852A>C	ENSP00000498393.1:n.*852A>C
ENST00000651455.1:c.*554A>C	ENSP00000498963.1:n.*554A>C
ENST00000674797.2:c.1462A>C	ENSP00000502299.2:p.Lys488Gln
ENST00000679569.1:n.2124A>C
ENST00000679842.1:c.1810A>C	ENSP00000506109.1:p.Lys604Gln
ENST00000680454.1:n.2254A>C
ENST00000681102.1:c.1630A>C	ENSP00000505600.1:p.Lys544Gln
ENST00000681177.1:c.1516-7198A>C	ENSP00000506327.1:n.1516-7198A>C
ENST00000681937.1:n.2148-7198A>C
ENST00000366576.3:c.472A>C	ENSP00000355535.3:p.Lys158Gln
ENST00000366577.9:c.1810A>C	ENSP00000355536.5:p.Lys604Gln
ENST00000463959.1:n.1829A>C
ENST00000535889.5:c.1810A>C	ENSP00000441845.1:p.Lys604Gln
NM_000254.2:c.1810A>C	NP_000245.2:p.Lys604Gln
NM_001291939.1:c.1810A>C	NP_001278868.1:p.Lys604Gln
NM_001291940.1:c.589A>C	NP_001278869.1:p.Lys197Gln
XM_005273141.3:c.1807A>C	XP_005273198.1:p.Lys603Gln
XM_006711769.2:c.1810A>C	XP_006711832.1:p.Lys604Gln
XM_006711770.1:c.874A>C	XP_006711833.1:p.Lys292Gln
XM_011544193.1:c.1810A>C	XP_011542495.1:p.Lys604Gln
XM_011544194.1:c.1978A>C	XP_011542496.1:p.Lys660Gln
XM_005273141.5:c.1807A>C	XP_005273198.1:p.Lys603Gln
XM_006711770.3:c.874A>C	XP_006711833.1:p.Lys292Gln
XM_011544194.3:c.1978A>C	XP_011542496.1:p.Lys660Gln
XM_017001329.2:c.1978A>C	XP_016856818.1:p.Lys660Gln
XM_017001330.2:c.1978A>C	XP_016856819.1:p.Lys660Gln
NM_001291940.2:c.589A>C	NP_001278869.1:p.Lys197Gln
NM_000254.3:c.1810A>C MANE Select	NP_000245.2:p.Lys604Gln