Canonical Allele Identifier: CA2574163107

Gene: MTR

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236885134del , CM000663.2:g.236885134del	GRCh38
NC_000001.10:g.237048434del , CM000663.1:g.237048434del	GRCh37
NC_000001.9:g.235115057del	NCBI36
NG_008959.1:g.94854del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.2690del MANE Select	ENSP00000355536.5:p.Leu897Ter
ENST00000535889.6:c.2537del	ENSP00000441845.1:p.Leu846Ter
ENST00000650888.1:c.*1732del	ENSP00000498393.1:n.*1732del
ENST00000651455.1:c.*1434del	ENSP00000498963.1:n.*1434del
ENST00000674797.2:c.2342del	ENSP00000502299.2:p.Leu781Ter
ENST00000679569.1:n.3004del
ENST00000679842.1:c.2501del	ENSP00000506109.1:p.Leu834Ter
ENST00000680454.1:n.3134del
ENST00000681102.1:c.2510del	ENSP00000505600.1:p.Leu837Ter
ENST00000681177.1:c.2252del	ENSP00000506327.1:p.Leu751Ter
ENST00000681937.1:n.2884del
ENST00000366576.3:c.1352del	ENSP00000355535.3:p.Leu451Ter
ENST00000366577.9:c.2690del	ENSP00000355536.5:p.Leu897Ter
ENST00000535889.5:c.2537del	ENSP00000441845.1:p.Leu846Ter
NM_000254.2:c.2690del	NP_000245.2:p.Leu897Ter
NM_001291939.1:c.2537del	NP_001278868.1:p.Leu846Ter
NM_001291940.1:c.1469del	NP_001278869.1:p.Leu490Ter
XM_005273141.3:c.2687del	XP_005273198.1:p.Leu896Ter
XM_006711769.2:c.2690del	XP_006711832.1:p.Leu897Ter
XM_006711770.1:c.1754del	XP_006711833.1:p.Leu585Ter
XM_011544193.1:c.2501del	XP_011542495.1:p.Leu834Ter
XM_011544194.1:c.2858del	XP_011542496.1:p.Leu953Ter
XM_005273141.5:c.2687del	XP_005273198.1:p.Leu896Ter
XM_006711770.3:c.1754del	XP_006711833.1:p.Leu585Ter
XM_011544194.3:c.2858del	XP_011542496.1:p.Leu953Ter
XM_017001329.2:c.2705del	XP_016856818.1:p.Leu902Ter
XM_017001330.2:c.2669del	XP_016856819.1:p.Leu890Ter
NM_001291940.2:c.1469del	NP_001278869.1:p.Leu490Ter
NM_000254.3:c.2690del MANE Select	NP_000245.2:p.Leu897Ter