Canonical Allele Identifier: CA334066

Gene: MTMR2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.95923941G>C , CM000673.2:g.95923941G>C	GRCh38
NC_000011.9:g.95657105G>C , CM000673.1:g.95657105G>C	GRCh37
NC_000011.8:g.95296753G>C	NCBI36
NG_008333.1:g.5267C>G , LRG_257:g.5267C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346299.10:c.14C>G MANE Select	ENSP00000345752.6:p.Ser5Trp
ENST00000393223.8:c.-295C>G	ENSP00000376915.3:n.-295C>G
ENST00000481642.6:c.-431C>G	ENSP00000502505.1:n.-431C>G
ENST00000674950.1:c.14C>G	ENSP00000502425.1:p.Ser5Trp
ENST00000674974.1:c.14C>G	ENSP00000502337.1:p.Ser5Trp
ENST00000674989.1:c.-271C>G	ENSP00000502829.1:n.-271C>G
ENST00000675022.1:c.14C>G	ENSP00000502722.1:p.Ser5Trp
ENST00000675024.1:n.167C>G
ENST00000675030.1:c.14C>G	ENSP00000502386.1:p.Ser5Trp
ENST00000675174.1:c.-324C>G	ENSP00000502032.1:n.-324C>G
ENST00000675320.1:c.14C>G	ENSP00000502076.1:p.Ser5Trp
ENST00000675362.1:c.-368C>G	ENSP00000501989.1:n.-368C>G
ENST00000675489.1:c.-470C>G	ENSP00000501702.1:n.-470C>G
ENST00000675495.1:n.191C>G
ENST00000675652.1:c.-168C>G	ENSP00000502694.1:n.-168C>G
ENST00000675767.1:n.161C>G
ENST00000675848.1:c.-567C>G	ENSP00000502057.1:n.-567C>G
ENST00000675896.1:c.14C>G	ENSP00000502487.1:p.Ser5Trp
ENST00000675910.1:c.14C>G	ENSP00000502622.1:p.Ser5Trp
ENST00000675922.1:c.14C>G	ENSP00000502168.1:p.Ser5Trp
ENST00000676027.1:c.-640C>G	ENSP00000502405.1:n.-640C>G
ENST00000676146.1:c.14C>G	ENSP00000502583.1:p.Ser5Trp
ENST00000676177.1:c.14C>G	ENSP00000501635.1:p.Ser5Trp
ENST00000676261.1:c.-397C>G	ENSP00000501675.1:n.-397C>G
ENST00000676268.1:c.14C>G	ENSP00000502444.1:p.Ser5Trp
ENST00000676272.1:c.-97C>G	ENSP00000501601.1:n.-97C>G
ENST00000676388.1:c.14C>G	ENSP00000501866.1:p.Ser5Trp
ENST00000676432.1:n.160C>G
ENST00000346299.9:c.14C>G	ENSP00000345752.5:p.Ser5Trp
ENST00000352297.11:c.-274C>G	ENSP00000343737.7:n.-274C>G
ENST00000393223.7:c.-203C>G	ENSP00000376915.3:n.-203C>G
ENST00000409459.5:c.-347C>G	ENSP00000386882.1:n.-347C>G
ENST00000470011.5:n.250C>G
ENST00000481642.5:n.167C>G
NM_001243571.1:c.-470C>G	NP_001230500.1:n.-470C>G
NM_016156.5:c.14C>G , LRG_257t1:c.14C>G	NP_057240.3:p.Ser5Trp
NM_201278.2:c.-397C>G	NP_958435.1:n.-397C>G
NM_201281.2:c.-274C>G	NP_958438.1:n.-274C>G
XM_005274375.1:c.-326C>G	XP_005274432.1:n.-326C>G
XM_006718934.1:c.-347C>G	XP_006718997.1:n.-347C>G
XM_006718936.2:c.-276C>G	XP_006718999.1:n.-276C>G
XM_011543058.1:c.-356C>G	XP_011541360.1:n.-356C>G
XM_005274375.3:c.-326C>G	XP_005274432.1:n.-326C>G
NM_001243571.2:c.-470C>G	NP_001230500.1:n.-470C>G
NM_016156.6:c.14C>G MANE Select	NP_057240.3:p.Ser5Trp
NM_201278.3:c.-397C>G	NP_958435.1:n.-397C>G
NM_201281.3:c.-274C>G	NP_958438.1:n.-274C>G