Canonical Allele Identifier: CA2240124

Gene: MTMR14

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.9649622G>A , CM000665.2:g.9649622G>A	GRCh38
NC_000003.11:g.9691306G>A , CM000665.1:g.9691306G>A	GRCh37
NC_000003.10:g.9666306G>A	NCBI36
NG_017068.1:g.5190G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296003.9:c.39G>A MANE Select	ENSP00000296003.5:p.Ala13=
ENST00000296003.8:c.39G>A	ENSP00000296003.4:p.Ala13=
ENST00000351233.9:c.39G>A	ENSP00000334070.7:p.Ala13=
ENST00000353332.9:c.39G>A	ENSP00000323462.8:p.Ala13=
ENST00000416864.5:c.39G>A	ENSP00000412644.1:p.Ala13=
ENST00000420925.5:c.39G>A	ENSP00000401993.1:p.Ala13=
ENST00000430020.5:c.39G>A	ENSP00000392690.1:p.Ala13=
ENST00000437997.1:c.39G>A	ENSP00000408813.1:p.Ala13=
ENST00000447144.5:c.39G>A	ENSP00000410761.1:p.Ala13=
ENST00000480578.1:n.14G>A
ENST00000617504.4:c.39G>A	ENSP00000478236.1:p.Ala13=
NM_001077525.2:c.39G>A	NP_001070993.1:p.Ala13=
NM_001077526.2:c.39G>A	NP_001070994.1:p.Ala13=
NM_022485.4:c.39G>A	NP_071930.2:p.Ala13=
XM_005265400.1:c.39G>A	XP_005265457.1:p.Ala13=
XM_011534012.1:c.-95G>A	XP_011532314.1:n.-95G>A
XR_245152.1:n.163G>A
XM_005265400.2:c.39G>A	XP_005265457.1:p.Ala13=
XM_017007034.1:c.-95G>A	XP_016862523.1:n.-95G>A
XM_017007035.1:c.-95G>A	XP_016862524.1:n.-95G>A
XM_017007036.1:c.-95G>A	XP_016862525.1:n.-95G>A
XM_017007037.1:c.-95G>A	XP_016862526.1:n.-95G>A
XM_017007038.2:c.39G>A	XP_016862527.1:p.Ala13=
XM_017007039.1:c.-95G>A	XP_016862528.1:n.-95G>A
XM_017007040.1:c.-95G>A	XP_016862529.1:n.-95G>A
XM_017007041.1:c.-95G>A	XP_016862530.1:n.-95G>A
XM_017007042.2:c.39G>A	XP_016862531.1:p.Ala13=
XM_017007043.1:c.-95G>A	XP_016862532.1:n.-95G>A
XM_017007044.2:c.-528G>A	XP_016862533.1:n.-528G>A
XM_017007045.2:c.-467G>A	XP_016862534.1:n.-467G>A
XM_024453710.1:c.-467G>A	XP_024309478.1:n.-467G>A
XR_001740231.1:n.157G>A
XR_001740232.1:n.158G>A
XR_001740233.2:n.150G>A
XR_245152.2:n.150G>A
NM_001077525.3:c.39G>A MANE Select	NP_001070993.1:p.Ala13=
NM_001077526.3:c.39G>A	NP_001070994.1:p.Ala13=
NM_022485.5:c.39G>A	NP_071930.2:p.Ala13=
NM_001400518.1:c.-95G>A	NP_001387447.1:n.-95G>A
NM_001400519.1:c.39G>A	NP_001387448.1:p.Ala13=
NM_001400520.1:c.39G>A	NP_001387449.1:p.Ala13=
NM_001400521.1:c.-95G>A	NP_001387450.1:n.-95G>A
NM_001400522.1:c.39G>A	NP_001387451.1:p.Ala13=
NM_001400523.1:c.39G>A	NP_001387452.1:p.Ala13=
NM_001400524.1:c.39G>A	NP_001387453.1:p.Ala13=
NM_001400525.1:c.-95G>A	NP_001387454.1:n.-95G>A
NM_001400526.1:c.-95G>A	NP_001387455.1:n.-95G>A
NM_001400527.1:c.39G>A	NP_001387456.1:p.Ala13=
NM_001400528.1:c.39G>A	NP_001387457.1:p.Ala13=
NM_001400529.1:c.-95G>A	NP_001387458.1:n.-95G>A
NM_001400530.1:c.39G>A	NP_001387459.1:p.Ala13=
NM_001400531.1:c.39G>A	NP_001387460.1:p.Ala13=
NM_001400532.1:c.-95G>A	NP_001387461.1:n.-95G>A
NM_001400533.1:c.-467G>A	NP_001387462.1:n.-467G>A
NM_001400534.1:c.-528G>A	NP_001387463.1:n.-528G>A
NM_001400535.1:c.-318G>A	NP_001387464.1:n.-318G>A
NM_001400536.1:c.39G>A	NP_001387465.1:p.Ala13=
NM_001400537.1:c.-95G>A	NP_001387466.1:n.-95G>A
NM_001400538.1:c.-528G>A	NP_001387467.1:n.-528G>A
NM_001400539.1:c.-467G>A	NP_001387468.1:n.-467G>A
NM_001400540.1:c.-495G>A	NP_001387469.1:n.-495G>A
NM_001400541.1:c.-528G>A	NP_001387470.1:n.-528G>A
NM_001400542.1:c.-730G>A	NP_001387471.1:n.-730G>A
NM_001400543.1:c.-289G>A	NP_001387472.1:n.-289G>A
NM_001400544.1:c.-540G>A	NP_001387473.1:n.-540G>A
NM_001400545.1:c.-467G>A	NP_001387474.1:n.-467G>A
NM_001400546.1:c.-528G>A	NP_001387475.1:n.-528G>A
NM_001400547.1:c.-677G>A	NP_001387476.1:n.-677G>A
NM_001400548.1:c.-601G>A	NP_001387477.1:n.-601G>A
NM_001400549.1:c.-528G>A	NP_001387478.1:n.-528G>A
NM_001400550.1:c.-431G>A	NP_001387479.1:n.-431G>A
NR_174503.1:n.118G>A
NR_174504.1:n.118G>A
NR_174505.1:n.118G>A
NR_174506.1:n.118G>A
NR_174507.1:n.118G>A
NR_174508.1:n.118G>A
NR_174509.1:n.118G>A
NR_174510.1:n.118G>A
NR_174511.1:n.118G>A