Canonical Allele Identifier: CA2478943997
Gene: MTMR11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149930298T= , CM000663.2:g.149930298T= GRCh38
NC_000001.10:g.149902190T= , CM000663.1:g.149902190T= GRCh37
NC_000001.9:g.148168814T= NCBI36
NG_032777.1:g.2955A=

Transcript Alleles

HGVS Amino-acid change
ENST00000439741.4:c.1647+67A= MANE Select ENSP00000391668.2:n.1647+67A=
ENST00000369140.7:c.1431+67A= ENSP00000358136.3:n.1431+67A=
ENST00000439741.2:c.1647+67A= ENSP00000391668.2:n.1647+67A=
ENST00000466496.5:n.967+67A=
ENST00000482025.5:n.1873+67A=
ENST00000482343.5:n.1471+67A=
ENST00000490310.1:n.846A=
ENST00000492824.5:n.2067+67A=
ENST00000495054.1:n.690+67A=
NM_001145862.1:c.1647+67A= NP_001139334.1:n.1647+67A=
NM_181873.3:c.1431+67A= NP_870988.2:n.1431+67A=
XM_006711135.1:c.1539+67A= XP_006711198.1:n.1539+67A=
XM_006711136.2:c.1431+67A= XP_006711199.1:n.1431+67A=
XM_006711137.1:c.1431+67A= XP_006711200.1:n.1431+67A=
XM_011509098.1:c.1563+67A= XP_011507400.1:n.1563+67A=
XM_011509099.1:c.*672A= XP_011507401.1:n.*672A=
XR_426759.2:n.1838+67A=
XR_426760.2:n.1744+67A=
XM_011509099.3:c.*672A= XP_011507401.1:n.*672A=
XM_024452577.1:c.1563+67A= XP_024308345.1:n.1563+67A=
XM_024452578.1:c.1539+67A= XP_024308346.1:n.1539+67A=
XR_002959043.1:n.1860+67A=
XR_002959062.1:n.1976+67A=
XR_002959066.1:n.1678+67A=
XR_002959067.1:n.3197+67A=
XR_426760.4:n.1766+67A=
NM_001145862.2:c.1647+67A= MANE Select NP_001139334.1:n.1647+67A=