Canonical Allele Identifier: CA345375040

Gene: MTR

Linked Data

• gnomAD v4: 1-236852967-T-C
• MyVariant Identifiers: chr1:g.237016267T>C (hg19) ; chr1:g.236852967T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852967T>C , CM000663.2:g.236852967T>C	GRCh38
NC_000001.10:g.237016267T>C , CM000663.1:g.237016267T>C	GRCh37
NC_000001.9:g.235082890T>C	NCBI36
NG_008959.1:g.62687T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1832T>C MANE Select	ENSP00000355536.5:p.Ile611Thr
ENST00000535889.6:c.1832T>C	ENSP00000441845.1:p.Ile611Thr
ENST00000650888.1:c.*874T>C	ENSP00000498393.1:n.*874T>C
ENST00000651455.1:c.*576T>C	ENSP00000498963.1:n.*576T>C
ENST00000674797.2:c.1484T>C	ENSP00000502299.2:p.Ile495Thr
ENST00000679569.1:n.2146T>C
ENST00000679842.1:c.1832T>C	ENSP00000506109.1:p.Ile611Thr
ENST00000680454.1:n.2276T>C
ENST00000681102.1:c.1652T>C	ENSP00000505600.1:p.Ile551Thr
ENST00000681177.1:c.1516-6866T>C	ENSP00000506327.1:n.1516-6866T>C
ENST00000681937.1:n.2148-6866T>C
ENST00000366576.3:c.494T>C	ENSP00000355535.3:p.Ile165Thr
ENST00000366577.9:c.1832T>C	ENSP00000355536.5:p.Ile611Thr
ENST00000463959.1:n.1851T>C
ENST00000535889.5:c.1832T>C	ENSP00000441845.1:p.Ile611Thr
NM_000254.2:c.1832T>C	NP_000245.2:p.Ile611Thr
NM_001291939.1:c.1832T>C	NP_001278868.1:p.Ile611Thr
NM_001291940.1:c.611T>C	NP_001278869.1:p.Ile204Thr
XM_005273141.3:c.1829T>C	XP_005273198.1:p.Ile610Thr
XM_006711769.2:c.1832T>C	XP_006711832.1:p.Ile611Thr
XM_006711770.1:c.896T>C	XP_006711833.1:p.Ile299Thr
XM_011544193.1:c.1832T>C	XP_011542495.1:p.Ile611Thr
XM_011544194.1:c.2000T>C	XP_011542496.1:p.Ile667Thr
XM_005273141.5:c.1829T>C	XP_005273198.1:p.Ile610Thr
XM_006711770.3:c.896T>C	XP_006711833.1:p.Ile299Thr
XM_011544194.3:c.2000T>C	XP_011542496.1:p.Ile667Thr
XM_017001329.2:c.2000T>C	XP_016856818.1:p.Ile667Thr
XM_017001330.2:c.2000T>C	XP_016856819.1:p.Ile667Thr
NM_001291940.2:c.611T>C	NP_001278869.1:p.Ile204Thr
NM_000254.3:c.1832T>C MANE Select	NP_000245.2:p.Ile611Thr