Canonical Allele Identifier: CA39763170

Gene: MTR

Linked Data

• dbSNP Id: rs996946111
• gnomAD v2: 1-237044006-G-A
• gnomAD v3: 1-236880706-G-A
• gnomAD v4: 1-236880706-G-A
• MyVariant Identifiers: chr1:g.237044006G>A (hg19) ; chr1:g.236880706G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236880706G>A , CM000663.2:g.236880706G>A	GRCh38
NC_000001.10:g.237044006G>A , CM000663.1:g.237044006G>A	GRCh37
NC_000001.9:g.235110629G>A	NCBI36
NG_008959.1:g.90426G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000366577.10:c.2595-49G>A MANE Select	ENSP00000355536.5:n.2595-49G>A
ENST00000535889.6:c.2442-49G>A	ENSP00000441845.1:n.2442-49G>A
ENST00000650888.1:c.*1637-49G>A	ENSP00000498393.1:n.*1637-49G>A
ENST00000651455.1:c.*1339-49G>A	ENSP00000498963.1:n.*1339-49G>A
ENST00000674797.2:c.2247-49G>A	ENSP00000502299.2:n.2247-49G>A
ENST00000679569.1:n.2909-49G>A
ENST00000679842.1:c.2406-49G>A	ENSP00000506109.1:n.2406-49G>A
ENST00000680454.1:n.3039-49G>A
ENST00000681102.1:c.2415-49G>A	ENSP00000505600.1:n.2415-49G>A
ENST00000681177.1:c.2157-49G>A	ENSP00000506327.1:n.2157-49G>A
ENST00000681937.1:n.2789-49G>A
ENST00000366576.3:c.1257-49G>A	ENSP00000355535.3:n.1257-49G>A
ENST00000366577.9:c.2595-49G>A	ENSP00000355536.5:n.2595-49G>A
ENST00000535889.5:c.2442-49G>A	ENSP00000441845.1:n.2442-49G>A
NM_000254.2:c.2595-49G>A	NP_000245.2:n.2595-49G>A
NM_001291939.1:c.2442-49G>A	NP_001278868.1:n.2442-49G>A
NM_001291940.1:c.1374-49G>A	NP_001278869.1:n.1374-49G>A
XM_005273141.3:c.2592-49G>A	XP_005273198.1:n.2592-49G>A
XM_006711769.2:c.2595-49G>A	XP_006711832.1:n.2595-49G>A
XM_006711770.1:c.1659-49G>A	XP_006711833.1:n.1659-49G>A
XM_011544193.1:c.2406-49G>A	XP_011542495.1:n.2406-49G>A
XM_011544194.1:c.2763-49G>A	XP_011542496.1:n.2763-49G>A
XM_005273141.5:c.2592-49G>A	XP_005273198.1:n.2592-49G>A
XM_006711770.3:c.1659-49G>A	XP_006711833.1:n.1659-49G>A
XM_011544194.3:c.2763-49G>A	XP_011542496.1:n.2763-49G>A
XM_017001329.2:c.2610-49G>A	XP_016856818.1:n.2610-49G>A
XM_017001330.2:c.2574-49G>A	XP_016856819.1:n.2574-49G>A
NM_001291940.2:c.1374-49G>A	NP_001278869.1:n.1374-49G>A
NM_000254.3:c.2595-49G>A MANE Select	NP_000245.2:n.2595-49G>A