Canonical Allele Identifier: CA10640525

Gene: MTMR2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.95834303A>G , CM000673.2:g.95834303A>G	GRCh38
NC_000011.9:g.95567467A>G , CM000673.1:g.95567467A>G	GRCh37
NC_000011.8:g.95207115A>G	NCBI36
NG_008333.1:g.94905T>C , LRG_257:g.94905T>C
NG_029829.1:g.48843A>G , LRG_526:g.48843A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346299.10:c.*987T>C MANE Select	ENSP00000345752.6:n.*987T>C
ENST00000393223.8:c.*987T>C	ENSP00000376915.3:n.*987T>C
ENST00000674528.1:c.*987T>C	ENSP00000501567.1:n.*987T>C
ENST00000674610.1:c.*987T>C	ENSP00000501688.1:n.*987T>C
ENST00000674901.1:n.4057T>C
ENST00000674924.1:c.*987T>C	ENSP00000502433.1:n.*987T>C
ENST00000674950.1:c.*3108T>C	ENSP00000502425.1:n.*3108T>C
ENST00000674968.1:c.*987T>C	ENSP00000502567.1:n.*987T>C
ENST00000674974.1:c.*2854T>C	ENSP00000502337.1:n.*2854T>C
ENST00000674989.1:c.*987T>C	ENSP00000502829.1:n.*987T>C
ENST00000675022.1:c.*987T>C	ENSP00000502722.1:n.*987T>C
ENST00000675024.1:n.4090T>C
ENST00000675030.1:c.*6088T>C	ENSP00000502386.1:n.*6088T>C
ENST00000675034.1:n.4078T>C
ENST00000675174.1:c.*987T>C	ENSP00000502032.1:n.*987T>C
ENST00000675196.1:c.*987T>C	ENSP00000501867.1:n.*987T>C
ENST00000675237.1:n.4082T>C
ENST00000675288.1:c.*987T>C	ENSP00000501942.1:n.*987T>C
ENST00000675320.1:c.*2716T>C	ENSP00000502076.1:n.*2716T>C
ENST00000675362.1:c.*987T>C	ENSP00000501989.1:n.*987T>C
ENST00000675413.1:n.3880T>C
ENST00000675438.1:c.2610T>C	ENSP00000502388.1:n.2610T>C
ENST00000675454.1:c.*987T>C	ENSP00000501781.1:n.*987T>C
ENST00000675477.1:c.*987T>C	ENSP00000501751.1:n.*987T>C
ENST00000675489.1:c.*987T>C	ENSP00000501702.1:n.*987T>C
ENST00000675495.1:n.3991T>C
ENST00000675636.1:c.*987T>C	ENSP00000501850.1:n.*987T>C
ENST00000675652.1:c.*987T>C	ENSP00000502694.1:n.*987T>C
ENST00000675660.1:c.*987T>C	ENSP00000502824.1:n.*987T>C
ENST00000675767.1:n.3971T>C
ENST00000675807.1:c.*987T>C	ENSP00000501640.1:n.*987T>C
ENST00000675848.1:c.*987T>C	ENSP00000502057.1:n.*987T>C
ENST00000675896.1:c.*1814+1018T>C	ENSP00000502487.1:n.*1814+1018T>C
ENST00000675910.1:c.*2857T>C	ENSP00000502622.1:n.*2857T>C
ENST00000675922.1:c.*2810T>C	ENSP00000502168.1:n.*2810T>C
ENST00000675933.1:c.*987T>C	ENSP00000502575.1:n.*987T>C
ENST00000675957.1:n.3981T>C
ENST00000675981.1:c.*987T>C	ENSP00000502204.1:n.*987T>C
ENST00000676027.1:c.*987T>C	ENSP00000502405.1:n.*987T>C
ENST00000676146.1:c.*2530T>C	ENSP00000502583.1:n.*2530T>C
ENST00000676166.1:c.*987T>C	ENSP00000501632.1:n.*987T>C
ENST00000676177.1:c.*2832T>C	ENSP00000501635.1:n.*2832T>C
ENST00000676261.1:c.*987T>C	ENSP00000501675.1:n.*987T>C
ENST00000676268.1:c.*2237T>C	ENSP00000502444.1:n.*2237T>C
ENST00000676272.1:c.*987T>C	ENSP00000501601.1:n.*987T>C
ENST00000676378.1:c.*987T>C	ENSP00000502736.1:n.*987T>C
ENST00000676388.1:c.*2659T>C	ENSP00000501866.1:n.*2659T>C
ENST00000676393.1:n.3955T>C
ENST00000676432.1:n.4121T>C
ENST00000676440.1:c.*987T>C	ENSP00000501926.1:n.*987T>C
ENST00000346299.9:c.*987T>C	ENSP00000345752.5:n.*987T>C
ENST00000352297.11:c.*987T>C	ENSP00000343737.7:n.*987T>C
ENST00000393223.7:c.*987T>C	ENSP00000376915.3:n.*987T>C
ENST00000409459.5:c.*987T>C	ENSP00000386882.1:n.*987T>C
NM_001243571.1:c.*987T>C	NP_001230500.1:n.*987T>C
NM_016156.5:c.*987T>C , LRG_257t1:c.*987T>C	NP_057240.3:n.*987T>C
NM_201278.2:c.*987T>C	NP_958435.1:n.*987T>C
NM_201281.2:c.*987T>C	NP_958438.1:n.*987T>C
XM_005274374.1:c.*987T>C	XP_005274431.1:n.*987T>C
XM_005274375.1:c.*987T>C	XP_005274432.1:n.*987T>C
XM_006718934.1:c.*987T>C	XP_006718997.1:n.*987T>C
XM_006718935.1:c.*987T>C	XP_006718998.1:n.*987T>C
XM_006718936.2:c.*987T>C	XP_006718999.1:n.*987T>C
XM_011543058.1:c.*987T>C	XP_011541360.1:n.*987T>C
XM_011543059.1:c.*987T>C	XP_011541361.1:n.*987T>C
XM_005274374.3:c.*987T>C	XP_005274431.1:n.*987T>C
XM_005274375.3:c.*987T>C	XP_005274432.1:n.*987T>C
NM_001243571.2:c.*987T>C	NP_001230500.1:n.*987T>C
NM_016156.6:c.*987T>C MANE Select	NP_057240.3:n.*987T>C
NM_201278.3:c.*987T>C	NP_958435.1:n.*987T>C
NM_201281.3:c.*987T>C	NP_958438.1:n.*987T>C