Canonical Allele Identifier: CA10934743

Gene: MTR

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236795876C>T , CM000663.2:g.236795876C>T	GRCh38
NC_000001.10:g.236959176C>T , CM000663.1:g.236959176C>T	GRCh37
NC_000001.9:g.235025799C>T	NCBI36
NG_008959.1:g.5596C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366577.10:c.34+139C>T MANE Select	ENSP00000355536.5:n.34+139C>T
ENST00000535889.6:c.34+139C>T	ENSP00000441845.1:n.34+139C>T
ENST00000650888.1:c.34+139C>T	ENSP00000498393.1:n.34+139C>T
ENST00000651455.1:c.34+139C>T	ENSP00000498963.1:n.34+139C>T
ENST00000652435.1:c.-100+139C>T	ENSP00000505932.1:n.-100+139C>T
ENST00000674797.2:c.-100+139C>T	ENSP00000502299.2:n.-100+139C>T
ENST00000679569.1:n.351+139C>T
ENST00000679842.1:c.34+139C>T	ENSP00000506109.1:n.34+139C>T
ENST00000680454.1:n.478+139C>T
ENST00000681102.1:c.34+139C>T	ENSP00000505600.1:n.34+139C>T
ENST00000681177.1:c.34+139C>T	ENSP00000506327.1:n.34+139C>T
ENST00000366577.9:c.34+139C>T	ENSP00000355536.5:n.34+139C>T
ENST00000463959.1:n.123+139C>T
ENST00000535889.5:c.34+139C>T	ENSP00000441845.1:n.34+139C>T
NM_000254.2:c.34+139C>T	NP_000245.2:n.34+139C>T
NM_001291939.1:c.34+139C>T	NP_001278868.1:n.34+139C>T
NM_001291940.1:c.-1075+139C>T	NP_001278869.1:n.-1075+139C>T
XM_005273141.3:c.34+139C>T	XP_005273198.1:n.34+139C>T
XM_006711769.2:c.34+139C>T	XP_006711832.1:n.34+139C>T
XM_011544193.1:c.34+139C>T	XP_011542495.1:n.34+139C>T
XM_011544194.1:c.417+139C>T	XP_011542496.1:n.417+139C>T
XM_005273141.5:c.34+139C>T	XP_005273198.1:n.34+139C>T
XM_011544194.3:c.417+139C>T	XP_011542496.1:n.417+139C>T
XM_017001329.2:c.417+139C>T	XP_016856818.1:n.417+139C>T
XM_017001330.2:c.417+139C>T	XP_016856819.1:n.417+139C>T
NM_001291940.2:c.-1075+139C>T	NP_001278869.1:n.-1075+139C>T
NM_000254.3:c.34+139C>T MANE Select	NP_000245.2:n.34+139C>T