Canonical Allele Identifier: CA2651187198

Gene: MTR

Linked Data

• gnomAD v4: 1-236852422-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236852423del , CM000663.2:g.236852423del	GRCh38
NC_000001.10:g.237015723del , CM000663.1:g.237015723del	GRCh37
NC_000001.9:g.235082346del	NCBI36
NG_008959.1:g.62143del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.1696-98del MANE Select	ENSP00000355536.5:n.1696-98del
ENST00000535889.6:c.1696-98del	ENSP00000441845.1:n.1696-98del
ENST00000650888.1:c.*738-98del	ENSP00000498393.1:n.*738-98del
ENST00000651455.1:c.*440-98del	ENSP00000498963.1:n.*440-98del
ENST00000674797.2:c.1348-98del	ENSP00000502299.2:n.1348-98del
ENST00000679569.1:n.2010-98del
ENST00000679842.1:c.1696-98del	ENSP00000506109.1:n.1696-98del
ENST00000680454.1:n.2140-98del
ENST00000681102.1:c.1516-98del	ENSP00000505600.1:n.1516-98del
ENST00000681177.1:c.1516-7410del	ENSP00000506327.1:n.1516-7410del
ENST00000681937.1:n.2148-7410del
ENST00000366576.3:c.358-98del	ENSP00000355535.3:n.358-98del
ENST00000366577.9:c.1696-98del	ENSP00000355536.5:n.1696-98del
ENST00000463959.1:n.1715-98del
ENST00000535889.5:c.1696-98del	ENSP00000441845.1:n.1696-98del
NM_000254.2:c.1696-98del	NP_000245.2:n.1696-98del
NM_001291939.1:c.1696-98del	NP_001278868.1:n.1696-98del
NM_001291940.1:c.475-98del	NP_001278869.1:n.475-98del
XM_005273141.3:c.1693-98del	XP_005273198.1:n.1693-98del
XM_006711769.2:c.1696-98del	XP_006711832.1:n.1696-98del
XM_006711770.1:c.760-98del	XP_006711833.1:n.760-98del
XM_011544193.1:c.1696-98del	XP_011542495.1:n.1696-98del
XM_011544194.1:c.1864-98del	XP_011542496.1:n.1864-98del
XM_005273141.5:c.1693-98del	XP_005273198.1:n.1693-98del
XM_006711770.3:c.760-98del	XP_006711833.1:n.760-98del
XM_011544194.3:c.1864-98del	XP_011542496.1:n.1864-98del
XM_017001329.2:c.1864-98del	XP_016856818.1:n.1864-98del
XM_017001330.2:c.1864-98del	XP_016856819.1:n.1864-98del
NM_001291940.2:c.475-98del	NP_001278869.1:n.475-98del
NM_000254.3:c.1696-98del MANE Select	NP_000245.2:n.1696-98del