Canonical Allele Identifier: CA2487090316

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852494_236852496delinsCTT , CM000663.2:g.236852494_236852496delinsCTT	GRCh38
NC_000001.10:g.237015794_237015796delinsCTT , CM000663.1:g.237015794_237015796delinsCTT	GRCh37
NC_000001.9:g.235082417_235082419delinsCTT	NCBI36
NG_008959.1:g.62214_62216delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1696-27_1696-25delinsCTT MANE Select	ENSP00000355536.5:n.1696-27_1696-25delinsCTT
ENST00000535889.6:c.1696-27_1696-25delinsCTT	ENSP00000441845.1:n.1696-27_1696-25delinsCTT
ENST00000650888.1:c.*738-27_*738-25delinsCTT	ENSP00000498393.1:n.*738-27_*738-25delinsCTT
ENST00000651455.1:c.*440-27_*440-25delinsCTT	ENSP00000498963.1:n.*440-27_*440-25delinsCTT
ENST00000674797.2:c.1348-27_1348-25delinsCTT	ENSP00000502299.2:n.1348-27_1348-25delinsCTT
ENST00000679569.1:n.2010-27_2010-25delinsCTT
ENST00000679842.1:c.1696-27_1696-25delinsCTT	ENSP00000506109.1:n.1696-27_1696-25delinsCTT
ENST00000680454.1:n.2140-27_2140-25delinsCTT
ENST00000681102.1:c.1516-27_1516-25delinsCTT	ENSP00000505600.1:n.1516-27_1516-25delinsCTT
ENST00000681177.1:c.1516-7339_1516-7337delinsCTT	ENSP00000506327.1:n.1516-7339_1516-7337delinsCTT
ENST00000681937.1:n.2148-7339_2148-7337delinsCTT
ENST00000366576.3:c.358-27_358-25delinsCTT	ENSP00000355535.3:n.358-27_358-25delinsCTT
ENST00000366577.9:c.1696-27_1696-25delinsCTT	ENSP00000355536.5:n.1696-27_1696-25delinsCTT
ENST00000463959.1:n.1715-27_1715-25delinsCTT
ENST00000535889.5:c.1696-27_1696-25delinsCTT	ENSP00000441845.1:n.1696-27_1696-25delinsCTT
NM_000254.2:c.1696-27_1696-25delinsCTT	NP_000245.2:n.1696-27_1696-25delinsCTT
NM_001291939.1:c.1696-27_1696-25delinsCTT	NP_001278868.1:n.1696-27_1696-25delinsCTT
NM_001291940.1:c.475-27_475-25delinsCTT	NP_001278869.1:n.475-27_475-25delinsCTT
XM_005273141.3:c.1693-27_1693-25delinsCTT	XP_005273198.1:n.1693-27_1693-25delinsCTT
XM_006711769.2:c.1696-27_1696-25delinsCTT	XP_006711832.1:n.1696-27_1696-25delinsCTT
XM_006711770.1:c.760-27_760-25delinsCTT	XP_006711833.1:n.760-27_760-25delinsCTT
XM_011544193.1:c.1696-27_1696-25delinsCTT	XP_011542495.1:n.1696-27_1696-25delinsCTT
XM_011544194.1:c.1864-27_1864-25delinsCTT	XP_011542496.1:n.1864-27_1864-25delinsCTT
XM_005273141.5:c.1693-27_1693-25delinsCTT	XP_005273198.1:n.1693-27_1693-25delinsCTT
XM_006711770.3:c.760-27_760-25delinsCTT	XP_006711833.1:n.760-27_760-25delinsCTT
XM_011544194.3:c.1864-27_1864-25delinsCTT	XP_011542496.1:n.1864-27_1864-25delinsCTT
XM_017001329.2:c.1864-27_1864-25delinsCTT	XP_016856818.1:n.1864-27_1864-25delinsCTT
XM_017001330.2:c.1864-27_1864-25delinsCTT	XP_016856819.1:n.1864-27_1864-25delinsCTT
NM_001291940.2:c.475-27_475-25delinsCTT	NP_001278869.1:n.475-27_475-25delinsCTT
NM_000254.3:c.1696-27_1696-25delinsCTT MANE Select	NP_000245.2:n.1696-27_1696-25delinsCTT