Canonical Allele Identifier: CA2487101807

Gene: MTR

Linked Data

• dbSNP Id: rs1665682877
• gnomAD v4: 1-236880703-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236880704del , CM000663.2:g.236880704del	GRCh38
NC_000001.10:g.237044004del , CM000663.1:g.237044004del	GRCh37
NC_000001.9:g.235110627del	NCBI36
NG_008959.1:g.90424del

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2595-51del MANE Select	ENSP00000355536.5:n.2595-51del
ENST00000535889.6:c.2442-51del	ENSP00000441845.1:n.2442-51del
ENST00000650888.1:c.*1637-51del	ENSP00000498393.1:n.*1637-51del
ENST00000651455.1:c.*1339-51del	ENSP00000498963.1:n.*1339-51del
ENST00000674797.2:c.2247-51del	ENSP00000502299.2:n.2247-51del
ENST00000679569.1:n.2909-51del
ENST00000679842.1:c.2406-51del	ENSP00000506109.1:n.2406-51del
ENST00000680454.1:n.3039-51del
ENST00000681102.1:c.2415-51del	ENSP00000505600.1:n.2415-51del
ENST00000681177.1:c.2157-51del	ENSP00000506327.1:n.2157-51del
ENST00000681937.1:n.2789-51del
ENST00000366576.3:c.1257-51del	ENSP00000355535.3:n.1257-51del
ENST00000366577.9:c.2595-51del	ENSP00000355536.5:n.2595-51del
ENST00000535889.5:c.2442-51del	ENSP00000441845.1:n.2442-51del
NM_000254.2:c.2595-51del	NP_000245.2:n.2595-51del
NM_001291939.1:c.2442-51del	NP_001278868.1:n.2442-51del
NM_001291940.1:c.1374-51del	NP_001278869.1:n.1374-51del
XM_005273141.3:c.2592-51del	XP_005273198.1:n.2592-51del
XM_006711769.2:c.2595-51del	XP_006711832.1:n.2595-51del
XM_006711770.1:c.1659-51del	XP_006711833.1:n.1659-51del
XM_011544193.1:c.2406-51del	XP_011542495.1:n.2406-51del
XM_011544194.1:c.2763-51del	XP_011542496.1:n.2763-51del
XM_005273141.5:c.2592-51del	XP_005273198.1:n.2592-51del
XM_006711770.3:c.1659-51del	XP_006711833.1:n.1659-51del
XM_011544194.3:c.2763-51del	XP_011542496.1:n.2763-51del
XM_017001329.2:c.2610-51del	XP_016856818.1:n.2610-51del
XM_017001330.2:c.2574-51del	XP_016856819.1:n.2574-51del
NM_001291940.2:c.1374-51del	NP_001278869.1:n.1374-51del
NM_000254.3:c.2595-51del MANE Select	NP_000245.2:n.2595-51del