Canonical Allele Identifier: CA69965279
Gene: MTMR14 HGNC NCBI

Linked Data

ClinVar Variation Id: 2689462
ClinVar RCV Id: RCV003488057
dbSNP Id: rs758937216
gnomAD v2: 3-9730631-G-T
gnomAD v3: 3-9688947-G-T
gnomAD v4: 3-9688947-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.9688947G>T , CM000665.2:g.9688947G>T GRCh38
NC_000003.11:g.9730631G>T , CM000665.1:g.9730631G>T GRCh37
NC_000003.10:g.9705631G>T NCBI36
NG_017068.1:g.44515G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000296003.9:c.1298G>T MANE Select ENSP00000296003.5:p.Arg433Leu
ENST00000296003.8:c.1298G>T ENSP00000296003.4:p.Arg433Leu
ENST00000351233.9:c.1298G>T ENSP00000334070.7:p.Arg433Leu
ENST00000353332.9:c.1298G>T ENSP00000323462.8:p.Arg433Leu
ENST00000414996.1:c.*655G>T ENSP00000392935.1:n.*655G>T
ENST00000420925.5:c.560G>T ENSP00000401993.1:p.Arg187Leu
ENST00000447144.5:c.*271G>T ENSP00000410761.1:n.*271G>T
ENST00000617504.4:c.1298G>T ENSP00000478236.1:p.Arg433Leu
NM_001077525.2:c.1298G>T NP_001070993.1:p.Arg433Leu
NM_001077526.2:c.1298G>T NP_001070994.1:p.Arg433Leu
NM_022485.4:c.1298G>T NP_071930.2:p.Arg433Leu
XM_005265400.1:c.1223G>T XP_005265457.1:p.Arg408Leu
XM_011534012.1:c.1016G>T XP_011532314.1:p.Arg339Leu
XM_011534013.1:c.935G>T XP_011532315.1:p.Arg312Leu
XR_245152.1:n.1422G>T
XM_005265400.2:c.1223G>T XP_005265457.1:p.Arg408Leu
XM_017007034.1:c.1367G>T XP_016862523.1:p.Arg456Leu
XM_017007035.1:c.1292G>T XP_016862524.1:p.Arg431Leu
XM_017007036.1:c.1367G>T XP_016862525.1:p.Arg456Leu
XM_017007037.1:c.1292G>T XP_016862526.1:p.Arg431Leu
XM_017007038.2:c.1223G>T XP_016862527.1:p.Arg408Leu
XM_017007039.1:c.1367G>T XP_016862528.1:p.Arg456Leu
XM_017007040.1:c.1292G>T XP_016862529.1:p.Arg431Leu
XM_017007041.1:c.941G>T XP_016862530.1:p.Arg314Leu
XM_017007042.2:c.1223G>T XP_016862531.1:p.Arg408Leu
XM_017007043.1:c.1016G>T XP_016862532.1:p.Arg339Leu
XM_017007044.2:c.581G>T XP_016862533.1:p.Arg194Leu
XM_017007045.2:c.656G>T XP_016862534.1:p.Arg219Leu
XM_024453709.1:c.935G>T XP_024309477.1:p.Arg312Leu
XM_024453710.1:c.656G>T XP_024309478.1:p.Arg219Leu
XR_001740231.1:n.1618G>T
XR_001740232.1:n.1544G>T
XR_001740233.2:n.1334G>T
XR_245152.2:n.1409G>T
NM_001077525.3:c.1298G>T MANE Select NP_001070993.1:p.Arg433Leu
NM_001077526.3:c.1298G>T NP_001070994.1:p.Arg433Leu
NM_022485.5:c.1298G>T NP_071930.2:p.Arg433Leu
NM_001400518.1:c.1367G>T NP_001387447.1:p.Arg456Leu
NM_001400519.1:c.1295G>T NP_001387448.1:p.Arg432Leu
NM_001400520.1:c.1223G>T NP_001387449.1:p.Arg408Leu
NM_001400521.1:c.1367G>T NP_001387450.1:p.Arg456Leu
NM_001400522.1:c.1295G>T NP_001387451.1:p.Arg432Leu
NM_001400523.1:c.1223G>T NP_001387452.1:p.Arg408Leu
NM_001400524.1:c.1052G>T NP_001387453.1:p.Arg351Leu
NM_001400525.1:c.1016G>T NP_001387454.1:p.Arg339Leu
NM_001400526.1:c.1292G>T NP_001387455.1:p.Arg431Leu
NM_001400527.1:c.1052G>T NP_001387456.1:p.Arg351Leu
NM_001400528.1:c.1223G>T NP_001387457.1:p.Arg408Leu
NM_001400529.1:c.1016G>T NP_001387458.1:p.Arg339Leu
NM_001400530.1:c.1052G>T NP_001387459.1:p.Arg351Leu
NM_001400531.1:c.1049G>T NP_001387460.1:p.Arg350Leu
NM_001400532.1:c.1016G>T NP_001387461.1:p.Arg339Leu
NM_001400533.1:c.656G>T NP_001387462.1:p.Arg219Leu
NM_001400534.1:c.656G>T NP_001387463.1:p.Arg219Leu
NM_001400535.1:c.656G>T NP_001387464.1:p.Arg219Leu
NM_001400536.1:c.977G>T NP_001387465.1:p.Arg326Leu
NM_001400537.1:c.941G>T NP_001387466.1:p.Arg314Leu
NM_001400538.1:c.581G>T NP_001387467.1:p.Arg194Leu
NM_001400539.1:c.656G>T NP_001387468.1:p.Arg219Leu
NM_001400540.1:c.656G>T NP_001387469.1:p.Arg219Leu
NM_001400541.1:c.656G>T NP_001387470.1:p.Arg219Leu
NM_001400542.1:c.656G>T NP_001387471.1:p.Arg219Leu
NM_001400543.1:c.656G>T NP_001387472.1:p.Arg219Leu
NM_001400544.1:c.437G>T NP_001387473.1:p.Arg146Leu
NM_001400545.1:c.656G>T NP_001387474.1:p.Arg219Leu
NM_001400546.1:c.656G>T NP_001387475.1:p.Arg219Leu
NM_001400547.1:c.437G>T NP_001387476.1:p.Arg146Leu
NM_001400548.1:c.437G>T NP_001387477.1:p.Arg146Leu
NM_001400549.1:c.581G>T NP_001387478.1:p.Arg194Leu
NM_001400550.1:c.437G>T NP_001387479.1:p.Arg146Leu
NR_174503.1:n.1302G>T
NR_174504.1:n.1377G>T
NR_174505.1:n.985G>T
NR_174506.1:n.1165G>T
NR_174507.1:n.1231G>T
NR_174508.1:n.1231G>T
NR_174509.1:n.1131G>T
NR_174510.1:n.1228G>T
NR_174511.1:n.1301G>T