Canonical Allele Identifier: CA2651189154

Gene: MTR

Linked Data

• gnomAD v4: 1-236885025-T-TCCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885025_236885026insCCTG , CM000663.2:g.236885025_236885026insCCTG	GRCh38
NC_000001.10:g.237048325_237048326insCCTG , CM000663.1:g.237048325_237048326insCCTG	GRCh37
NC_000001.9:g.235114948_235114949insCCTG	NCBI36
NG_008959.1:g.94745_94746insCCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2677-96_2677-95insCCTG MANE Select	ENSP00000355536.5:n.2677-96_2677-95insCCTG
ENST00000535889.6:c.2524-96_2524-95insCCTG	ENSP00000441845.1:n.2524-96_2524-95insCCTG
ENST00000650888.1:c.*1719-96_*1719-95insCCTG	ENSP00000498393.1:n.*1719-96_*1719-95insCCTG
ENST00000651455.1:c.*1421-96_*1421-95insCCTG	ENSP00000498963.1:n.*1421-96_*1421-95insCCTG
ENST00000674797.2:c.2329-96_2329-95insCCTG	ENSP00000502299.2:n.2329-96_2329-95insCCTG
ENST00000679569.1:n.2991-96_2991-95insCCTG
ENST00000679842.1:c.2488-96_2488-95insCCTG	ENSP00000506109.1:n.2488-96_2488-95insCCTG
ENST00000680454.1:n.3121-96_3121-95insCCTG
ENST00000681102.1:c.2497-96_2497-95insCCTG	ENSP00000505600.1:n.2497-96_2497-95insCCTG
ENST00000681177.1:c.2239-96_2239-95insCCTG	ENSP00000506327.1:n.2239-96_2239-95insCCTG
ENST00000681937.1:n.2871-96_2871-95insCCTG
ENST00000366576.3:c.1339-96_1339-95insCCTG	ENSP00000355535.3:n.1339-96_1339-95insCCTG
ENST00000366577.9:c.2677-96_2677-95insCCTG	ENSP00000355536.5:n.2677-96_2677-95insCCTG
ENST00000535889.5:c.2524-96_2524-95insCCTG	ENSP00000441845.1:n.2524-96_2524-95insCCTG
NM_000254.2:c.2677-96_2677-95insCCTG	NP_000245.2:n.2677-96_2677-95insCCTG
NM_001291939.1:c.2524-96_2524-95insCCTG	NP_001278868.1:n.2524-96_2524-95insCCTG
NM_001291940.1:c.1456-96_1456-95insCCTG	NP_001278869.1:n.1456-96_1456-95insCCTG
XM_005273141.3:c.2674-96_2674-95insCCTG	XP_005273198.1:n.2674-96_2674-95insCCTG
XM_006711769.2:c.2677-96_2677-95insCCTG	XP_006711832.1:n.2677-96_2677-95insCCTG
XM_006711770.1:c.1741-96_1741-95insCCTG	XP_006711833.1:n.1741-96_1741-95insCCTG
XM_011544193.1:c.2488-96_2488-95insCCTG	XP_011542495.1:n.2488-96_2488-95insCCTG
XM_011544194.1:c.2845-96_2845-95insCCTG	XP_011542496.1:n.2845-96_2845-95insCCTG
XM_005273141.5:c.2674-96_2674-95insCCTG	XP_005273198.1:n.2674-96_2674-95insCCTG
XM_006711770.3:c.1741-96_1741-95insCCTG	XP_006711833.1:n.1741-96_1741-95insCCTG
XM_011544194.3:c.2845-96_2845-95insCCTG	XP_011542496.1:n.2845-96_2845-95insCCTG
XM_017001329.2:c.2692-96_2692-95insCCTG	XP_016856818.1:n.2692-96_2692-95insCCTG
XM_017001330.2:c.2656-96_2656-95insCCTG	XP_016856819.1:n.2656-96_2656-95insCCTG
NM_001291940.2:c.1456-96_1456-95insCCTG	NP_001278869.1:n.1456-96_1456-95insCCTG
NM_000254.3:c.2677-96_2677-95insCCTG MANE Select	NP_000245.2:n.2677-96_2677-95insCCTG