Canonical Allele Identifier: CA1344854246
Gene: MTMR14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9688946C= , CM000665.2:g.9688946C= GRCh38
NC_000003.11:g.9730630C= , CM000665.1:g.9730630C= GRCh37
NC_000003.10:g.9705630C= NCBI36
NG_017068.1:g.44514C=

Transcript Alleles

HGVS Amino-acid change
ENST00000296003.9:c.1297C= MANE Select ENSP00000296003.5:p.Arg433=
ENST00000296003.8:c.1297C= ENSP00000296003.4:p.Arg433=
ENST00000351233.9:c.1297C= ENSP00000334070.7:p.Arg433=
ENST00000353332.9:c.1297C= ENSP00000323462.8:p.Arg433=
ENST00000414996.1:c.*654C= ENSP00000392935.1:n.*654C=
ENST00000420925.5:c.559C= ENSP00000401993.1:p.Arg187=
ENST00000447144.5:c.*270C= ENSP00000410761.1:n.*270C=
ENST00000617504.4:c.1297C= ENSP00000478236.1:p.Arg433=
NM_001077525.2:c.1297C= NP_001070993.1:p.Arg433=
NM_001077526.2:c.1297C= NP_001070994.1:p.Arg433=
NM_022485.4:c.1297C= NP_071930.2:p.Arg433=
XM_005265400.1:c.1222C= XP_005265457.1:p.Arg408=
XM_011534012.1:c.1015C= XP_011532314.1:p.Arg339=
XM_011534013.1:c.934C= XP_011532315.1:p.Arg312=
XR_245152.1:n.1421C=
XM_005265400.2:c.1222C= XP_005265457.1:p.Arg408=
XM_017007034.1:c.1366C= XP_016862523.1:p.Arg456=
XM_017007035.1:c.1291C= XP_016862524.1:p.Arg431=
XM_017007036.1:c.1366C= XP_016862525.1:p.Arg456=
XM_017007037.1:c.1291C= XP_016862526.1:p.Arg431=
XM_017007038.2:c.1222C= XP_016862527.1:p.Arg408=
XM_017007039.1:c.1366C= XP_016862528.1:p.Arg456=
XM_017007040.1:c.1291C= XP_016862529.1:p.Arg431=
XM_017007041.1:c.940C= XP_016862530.1:p.Arg314=
XM_017007042.2:c.1222C= XP_016862531.1:p.Arg408=
XM_017007043.1:c.1015C= XP_016862532.1:p.Arg339=
XM_017007044.2:c.580C= XP_016862533.1:p.Arg194=
XM_017007045.2:c.655C= XP_016862534.1:p.Arg219=
XM_024453709.1:c.934C= XP_024309477.1:p.Arg312=
XM_024453710.1:c.655C= XP_024309478.1:p.Arg219=
XR_001740231.1:n.1617C=
XR_001740232.1:n.1543C=
XR_001740233.2:n.1333C=
XR_245152.2:n.1408C=
NM_001077525.3:c.1297C= MANE Select NP_001070993.1:p.Arg433=
NM_001077526.3:c.1297C= NP_001070994.1:p.Arg433=
NM_022485.5:c.1297C= NP_071930.2:p.Arg433=
NM_001400518.1:c.1366C= NP_001387447.1:p.Arg456=
NM_001400519.1:c.1294C= NP_001387448.1:p.Arg432=
NM_001400520.1:c.1222C= NP_001387449.1:p.Arg408=
NM_001400521.1:c.1366C= NP_001387450.1:p.Arg456=
NM_001400522.1:c.1294C= NP_001387451.1:p.Arg432=
NM_001400523.1:c.1222C= NP_001387452.1:p.Arg408=
NM_001400524.1:c.1051C= NP_001387453.1:p.Arg351=
NM_001400525.1:c.1015C= NP_001387454.1:p.Arg339=
NM_001400526.1:c.1291C= NP_001387455.1:p.Arg431=
NM_001400527.1:c.1051C= NP_001387456.1:p.Arg351=
NM_001400528.1:c.1222C= NP_001387457.1:p.Arg408=
NM_001400529.1:c.1015C= NP_001387458.1:p.Arg339=
NM_001400530.1:c.1051C= NP_001387459.1:p.Arg351=
NM_001400531.1:c.1048C= NP_001387460.1:p.Arg350=
NM_001400532.1:c.1015C= NP_001387461.1:p.Arg339=
NM_001400533.1:c.655C= NP_001387462.1:p.Arg219=
NM_001400534.1:c.655C= NP_001387463.1:p.Arg219=
NM_001400535.1:c.655C= NP_001387464.1:p.Arg219=
NM_001400536.1:c.976C= NP_001387465.1:p.Arg326=
NM_001400537.1:c.940C= NP_001387466.1:p.Arg314=
NM_001400538.1:c.580C= NP_001387467.1:p.Arg194=
NM_001400539.1:c.655C= NP_001387468.1:p.Arg219=
NM_001400540.1:c.655C= NP_001387469.1:p.Arg219=
NM_001400541.1:c.655C= NP_001387470.1:p.Arg219=
NM_001400542.1:c.655C= NP_001387471.1:p.Arg219=
NM_001400543.1:c.655C= NP_001387472.1:p.Arg219=
NM_001400544.1:c.436C= NP_001387473.1:p.Arg146=
NM_001400545.1:c.655C= NP_001387474.1:p.Arg219=
NM_001400546.1:c.655C= NP_001387475.1:p.Arg219=
NM_001400547.1:c.436C= NP_001387476.1:p.Arg146=
NM_001400548.1:c.436C= NP_001387477.1:p.Arg146=
NM_001400549.1:c.580C= NP_001387478.1:p.Arg194=
NM_001400550.1:c.436C= NP_001387479.1:p.Arg146=
NR_174503.1:n.1301C=
NR_174504.1:n.1376C=
NR_174505.1:n.984C=
NR_174506.1:n.1164C=
NR_174507.1:n.1230C=
NR_174508.1:n.1230C=
NR_174509.1:n.1130C=
NR_174510.1:n.1227C=
NR_174511.1:n.1300C=