Canonical Allele Identifier: CA10584393

Gene: MTMR2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.95923875C>G , CM000673.2:g.95923875C>G	GRCh38
NC_000011.9:g.95657039C>G , CM000673.1:g.95657039C>G	GRCh37
NC_000011.8:g.95296687C>G	NCBI36
NG_008333.1:g.5333G>C , LRG_257:g.5333G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346299.10:c.80G>C MANE Select	ENSP00000345752.6:p.Ser27Thr
ENST00000393223.8:c.-229G>C	ENSP00000376915.3:n.-229G>C
ENST00000481642.6:c.-365G>C	ENSP00000502505.1:n.-365G>C
ENST00000674950.1:c.80G>C	ENSP00000502425.1:p.Ser27Thr
ENST00000674974.1:c.80G>C	ENSP00000502337.1:p.Ser27Thr
ENST00000674989.1:c.-205G>C	ENSP00000502829.1:n.-205G>C
ENST00000675022.1:c.80G>C	ENSP00000502722.1:p.Ser27Thr
ENST00000675024.1:n.233G>C
ENST00000675030.1:c.80G>C	ENSP00000502386.1:p.Ser27Thr
ENST00000675174.1:c.-258G>C	ENSP00000502032.1:n.-258G>C
ENST00000675196.1:c.-464G>C	ENSP00000501867.1:n.-464G>C
ENST00000675320.1:c.80G>C	ENSP00000502076.1:p.Ser27Thr
ENST00000675362.1:c.-302G>C	ENSP00000501989.1:n.-302G>C
ENST00000675489.1:c.-404G>C	ENSP00000501702.1:n.-404G>C
ENST00000675495.1:n.257G>C
ENST00000675652.1:c.-102G>C	ENSP00000502694.1:n.-102G>C
ENST00000675767.1:n.227G>C
ENST00000675848.1:c.-501G>C	ENSP00000502057.1:n.-501G>C
ENST00000675896.1:c.80G>C	ENSP00000502487.1:p.Ser27Thr
ENST00000675910.1:c.80G>C	ENSP00000502622.1:p.Ser27Thr
ENST00000675922.1:c.80G>C	ENSP00000502168.1:p.Ser27Thr
ENST00000676027.1:c.-574G>C	ENSP00000502405.1:n.-574G>C
ENST00000676146.1:c.80G>C	ENSP00000502583.1:p.Ser27Thr
ENST00000676177.1:c.80G>C	ENSP00000501635.1:p.Ser27Thr
ENST00000676261.1:c.-331G>C	ENSP00000501675.1:n.-331G>C
ENST00000676268.1:c.80G>C	ENSP00000502444.1:p.Ser27Thr
ENST00000676272.1:c.-31G>C	ENSP00000501601.1:n.-31G>C
ENST00000676388.1:c.80G>C	ENSP00000501866.1:p.Ser27Thr
ENST00000676432.1:n.226G>C
ENST00000346299.9:c.80G>C	ENSP00000345752.5:p.Ser27Thr
ENST00000352297.11:c.-208G>C	ENSP00000343737.7:n.-208G>C
ENST00000393223.7:c.-137G>C	ENSP00000376915.3:n.-137G>C
ENST00000409459.5:c.-281G>C	ENSP00000386882.1:n.-281G>C
ENST00000470011.5:n.316G>C
ENST00000481642.5:n.233G>C
NM_001243571.1:c.-404G>C	NP_001230500.1:n.-404G>C
NM_016156.5:c.80G>C , LRG_257t1:c.80G>C	NP_057240.3:p.Ser27Thr
NM_201278.2:c.-331G>C	NP_958435.1:n.-331G>C
NM_201281.2:c.-208G>C	NP_958438.1:n.-208G>C
XM_005274375.1:c.-260G>C	XP_005274432.1:n.-260G>C
XM_006718934.1:c.-281G>C	XP_006718997.1:n.-281G>C
XM_006718936.2:c.-210G>C	XP_006718999.1:n.-210G>C
XM_011543058.1:c.-290G>C	XP_011541360.1:n.-290G>C
XM_005274375.3:c.-260G>C	XP_005274432.1:n.-260G>C
NM_001243571.2:c.-404G>C	NP_001230500.1:n.-404G>C
NM_016156.6:c.80G>C MANE Select	NP_057240.3:p.Ser27Thr
NM_201278.3:c.-331G>C	NP_958435.1:n.-331G>C
NM_201281.3:c.-208G>C	NP_958438.1:n.-208G>C