Canonical Allele Identifier: CA2478944023
Gene: MTMR11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149930381C= , CM000663.2:g.149930381C= GRCh38
NC_000001.10:g.149902273C= , CM000663.1:g.149902273C= GRCh37
NC_000001.9:g.148168897C= NCBI36
NG_032777.1:g.2872G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000439741.4:c.1631G= MANE Select ENSP00000391668.2:p.Trp544=
ENST00000369140.7:c.1415G= ENSP00000358136.3:p.Trp472=
ENST00000439741.2:c.1631G= ENSP00000391668.2:p.Trp544=
ENST00000466496.5:n.951G=
ENST00000482025.5:n.1857G=
ENST00000482343.5:n.1455G=
ENST00000490310.1:n.763G=
ENST00000492824.5:n.2051G=
ENST00000495054.1:n.674G=
NM_001145862.1:c.1631G= NP_001139334.1:p.Trp544=
NM_181873.3:c.1415G= NP_870988.2:p.Trp472=
XM_006711135.1:c.1523G= XP_006711198.1:p.Trp508=
XM_006711136.2:c.1415G= XP_006711199.1:p.Trp472=
XM_006711137.1:c.1415G= XP_006711200.1:p.Trp472=
XM_011509098.1:c.1547G= XP_011507400.1:p.Trp516=
XM_011509099.1:c.*589G= XP_011507401.1:n.*589G=
XR_426759.2:n.1822G=
XR_426760.2:n.1728G=
XM_011509099.3:c.*589G= XP_011507401.1:n.*589G=
XM_024452577.1:c.1547G= XP_024308345.1:p.Trp516=
XM_024452578.1:c.1523G= XP_024308346.1:p.Trp508=
XR_002959043.1:n.1844G=
XR_002959062.1:n.1960G=
XR_002959066.1:n.1662G=
XR_002959067.1:n.3181G=
XR_426760.4:n.1750G=
NM_001145862.2:c.1631G= MANE Select NP_001139334.1:p.Trp544=