Canonical Allele Identifier: CA2487090461

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852885_236852887delinsGTT , CM000663.2:g.236852885_236852887delinsGTT	GRCh38
NC_000001.10:g.237016185_237016187delinsGTT , CM000663.1:g.237016185_237016187delinsGTT	GRCh37
NC_000001.9:g.235082808_235082810delinsGTT	NCBI36
NG_008959.1:g.62605_62607delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1813-63_1813-61delinsGTT MANE Select	ENSP00000355536.5:n.1813-63_1813-61delinsGTT
ENST00000535889.6:c.1813-63_1813-61delinsGTT	ENSP00000441845.1:n.1813-63_1813-61delinsGTT
ENST00000650888.1:c.*855-63_*855-61delinsGTT	ENSP00000498393.1:n.*855-63_*855-61delinsGTT
ENST00000651455.1:c.*557-63_*557-61delinsGTT	ENSP00000498963.1:n.*557-63_*557-61delinsGTT
ENST00000674797.2:c.1465-63_1465-61delinsGTT	ENSP00000502299.2:n.1465-63_1465-61delinsGTT
ENST00000679569.1:n.2127-63_2127-61delinsGTT
ENST00000679842.1:c.1813-63_1813-61delinsGTT	ENSP00000506109.1:n.1813-63_1813-61delinsGTT
ENST00000680454.1:n.2257-63_2257-61delinsGTT
ENST00000681102.1:c.1633-63_1633-61delinsGTT	ENSP00000505600.1:n.1633-63_1633-61delinsGTT
ENST00000681177.1:c.1516-6948_1516-6946delinsGTT	ENSP00000506327.1:n.1516-6948_1516-6946delinsGTT
ENST00000681937.1:n.2148-6948_2148-6946delinsGTT
ENST00000366576.3:c.475-63_475-61delinsGTT	ENSP00000355535.3:n.475-63_475-61delinsGTT
ENST00000366577.9:c.1813-63_1813-61delinsGTT	ENSP00000355536.5:n.1813-63_1813-61delinsGTT
ENST00000463959.1:n.1832-63_1832-61delinsGTT
ENST00000535889.5:c.1813-63_1813-61delinsGTT	ENSP00000441845.1:n.1813-63_1813-61delinsGTT
NM_000254.2:c.1813-63_1813-61delinsGTT	NP_000245.2:n.1813-63_1813-61delinsGTT
NM_001291939.1:c.1813-63_1813-61delinsGTT	NP_001278868.1:n.1813-63_1813-61delinsGTT
NM_001291940.1:c.592-63_592-61delinsGTT	NP_001278869.1:n.592-63_592-61delinsGTT
XM_005273141.3:c.1810-63_1810-61delinsGTT	XP_005273198.1:n.1810-63_1810-61delinsGTT
XM_006711769.2:c.1813-63_1813-61delinsGTT	XP_006711832.1:n.1813-63_1813-61delinsGTT
XM_006711770.1:c.877-63_877-61delinsGTT	XP_006711833.1:n.877-63_877-61delinsGTT
XM_011544193.1:c.1813-63_1813-61delinsGTT	XP_011542495.1:n.1813-63_1813-61delinsGTT
XM_011544194.1:c.1981-63_1981-61delinsGTT	XP_011542496.1:n.1981-63_1981-61delinsGTT
XM_005273141.5:c.1810-63_1810-61delinsGTT	XP_005273198.1:n.1810-63_1810-61delinsGTT
XM_006711770.3:c.877-63_877-61delinsGTT	XP_006711833.1:n.877-63_877-61delinsGTT
XM_011544194.3:c.1981-63_1981-61delinsGTT	XP_011542496.1:n.1981-63_1981-61delinsGTT
XM_017001329.2:c.1981-63_1981-61delinsGTT	XP_016856818.1:n.1981-63_1981-61delinsGTT
XM_017001330.2:c.1981-63_1981-61delinsGTT	XP_016856819.1:n.1981-63_1981-61delinsGTT
NM_001291940.2:c.592-63_592-61delinsGTT	NP_001278869.1:n.592-63_592-61delinsGTT
NM_000254.3:c.1813-63_1813-61delinsGTT MANE Select	NP_000245.2:n.1813-63_1813-61delinsGTT