Canonical Allele Identifier: CA2647759195
Gene: MTMR11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149930293_149930305dup , CM000663.2:g.149930293_149930305dup GRCh38
NC_000001.10:g.149902185_149902197dup , CM000663.1:g.149902185_149902197dup GRCh37
NC_000001.9:g.148168809_148168821dup NCBI36
NG_032777.1:g.2950_2962dup

Transcript Alleles

HGVS Amino-acid change
ENST00000439741.4:c.1647+62_1647+74dup MANE Select ENSP00000391668.2:n.1647+62_1647+74dup
ENST00000369140.7:c.1431+62_1431+74dup ENSP00000358136.3:n.1431+62_1431+74dup
ENST00000439741.2:c.1647+62_1647+74dup ENSP00000391668.2:n.1647+62_1647+74dup
ENST00000466496.5:n.967+62_967+74dup
ENST00000482025.5:n.1873+62_1873+74dup
ENST00000482343.5:n.1471+62_1471+74dup
ENST00000490310.1:n.841_853dup
ENST00000492824.5:n.2067+62_2067+74dup
ENST00000495054.1:n.690+62_690+74dup
NM_001145862.1:c.1647+62_1647+74dup NP_001139334.1:n.1647+62_1647+74dup
NM_181873.3:c.1431+62_1431+74dup NP_870988.2:n.1431+62_1431+74dup
XM_006711135.1:c.1539+62_1539+74dup XP_006711198.1:n.1539+62_1539+74dup
XM_006711136.2:c.1431+62_1431+74dup XP_006711199.1:n.1431+62_1431+74dup
XM_006711137.1:c.1431+62_1431+74dup XP_006711200.1:n.1431+62_1431+74dup
XM_011509098.1:c.1563+62_1563+74dup XP_011507400.1:n.1563+62_1563+74dup
XM_011509099.1:c.*667_*679dup XP_011507401.1:n.*667_*679dup
XR_426759.2:n.1838+62_1838+74dup
XR_426760.2:n.1744+62_1744+74dup
XM_011509099.3:c.*667_*679dup XP_011507401.1:n.*667_*679dup
XM_024452577.1:c.1563+62_1563+74dup XP_024308345.1:n.1563+62_1563+74dup
XM_024452578.1:c.1539+62_1539+74dup XP_024308346.1:n.1539+62_1539+74dup
XR_002959043.1:n.1860+62_1860+74dup
XR_002959062.1:n.1976+62_1976+74dup
XR_002959066.1:n.1678+62_1678+74dup
XR_002959067.1:n.3197+62_3197+74dup
XR_426760.4:n.1766+62_1766+74dup
NM_001145862.2:c.1647+62_1647+74dup MANE Select NP_001139334.1:n.1647+62_1647+74dup