Canonical Allele Identifier: CA2487090389

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852710_236852711delinsGC , CM000663.2:g.236852710_236852711delinsGC	GRCh38
NC_000001.10:g.237016010_237016011delinsGC , CM000663.1:g.237016010_237016011delinsGC	GRCh37
NC_000001.9:g.235082633_235082634delinsGC	NCBI36
NG_008959.1:g.62430_62431delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1812+73_1812+74delinsGC MANE Select	ENSP00000355536.5:n.1812+73_1812+74delinsGC
ENST00000535889.6:c.1812+73_1812+74delinsGC	ENSP00000441845.1:n.1812+73_1812+74delinsGC
ENST00000650888.1:c.*854+73_*854+74delinsGC	ENSP00000498393.1:n.*854+73_*854+74delinsGC
ENST00000651455.1:c.*556+73_*556+74delinsGC	ENSP00000498963.1:n.*556+73_*556+74delinsGC
ENST00000674797.2:c.1464+73_1464+74delinsGC	ENSP00000502299.2:n.1464+73_1464+74delinsGC
ENST00000679569.1:n.2126+73_2126+74delinsGC
ENST00000679842.1:c.1812+73_1812+74delinsGC	ENSP00000506109.1:n.1812+73_1812+74delinsGC
ENST00000680454.1:n.2256+73_2256+74delinsGC
ENST00000681102.1:c.1632+73_1632+74delinsGC	ENSP00000505600.1:n.1632+73_1632+74delinsGC
ENST00000681177.1:c.1516-7123_1516-7122delinsGC	ENSP00000506327.1:n.1516-7123_1516-7122delinsGC
ENST00000681937.1:n.2148-7123_2148-7122delinsGC
ENST00000366576.3:c.474+73_474+74delinsGC	ENSP00000355535.3:n.474+73_474+74delinsGC
ENST00000366577.9:c.1812+73_1812+74delinsGC	ENSP00000355536.5:n.1812+73_1812+74delinsGC
ENST00000463959.1:n.1831+73_1831+74delinsGC
ENST00000535889.5:c.1812+73_1812+74delinsGC	ENSP00000441845.1:n.1812+73_1812+74delinsGC
NM_000254.2:c.1812+73_1812+74delinsGC	NP_000245.2:n.1812+73_1812+74delinsGC
NM_001291939.1:c.1812+73_1812+74delinsGC	NP_001278868.1:n.1812+73_1812+74delinsGC
NM_001291940.1:c.591+73_591+74delinsGC	NP_001278869.1:n.591+73_591+74delinsGC
XM_005273141.3:c.1809+73_1809+74delinsGC	XP_005273198.1:n.1809+73_1809+74delinsGC
XM_006711769.2:c.1812+73_1812+74delinsGC	XP_006711832.1:n.1812+73_1812+74delinsGC
XM_006711770.1:c.876+73_876+74delinsGC	XP_006711833.1:n.876+73_876+74delinsGC
XM_011544193.1:c.1812+73_1812+74delinsGC	XP_011542495.1:n.1812+73_1812+74delinsGC
XM_011544194.1:c.1980+73_1980+74delinsGC	XP_011542496.1:n.1980+73_1980+74delinsGC
XM_005273141.5:c.1809+73_1809+74delinsGC	XP_005273198.1:n.1809+73_1809+74delinsGC
XM_006711770.3:c.876+73_876+74delinsGC	XP_006711833.1:n.876+73_876+74delinsGC
XM_011544194.3:c.1980+73_1980+74delinsGC	XP_011542496.1:n.1980+73_1980+74delinsGC
XM_017001329.2:c.1980+73_1980+74delinsGC	XP_016856818.1:n.1980+73_1980+74delinsGC
XM_017001330.2:c.1980+73_1980+74delinsGC	XP_016856819.1:n.1980+73_1980+74delinsGC
NM_001291940.2:c.591+73_591+74delinsGC	NP_001278869.1:n.591+73_591+74delinsGC
NM_000254.3:c.1812+73_1812+74delinsGC MANE Select	NP_000245.2:n.1812+73_1812+74delinsGC