Canonical Allele Identifier: CA2478943989

Gene: MTMR11

Linked Data

• dbSNP Id: rs2092641095

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.149930286_149930287insG , CM000663.2:g.149930286_149930287insG	GRCh38
NC_000001.10:g.149902178_149902179insG , CM000663.1:g.149902178_149902179insG	GRCh37
NC_000001.9:g.148168802_148168803insG	NCBI36
NG_032777.1:g.2966_2967insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439741.4:c.1647+78_1647+79insC MANE Select	ENSP00000391668.2:n.1647+78_1647+79insC
ENST00000369140.7:c.1431+78_1431+79insC	ENSP00000358136.3:n.1431+78_1431+79insC
ENST00000439741.2:c.1647+78_1647+79insC	ENSP00000391668.2:n.1647+78_1647+79insC
ENST00000466496.5:n.967+78_967+79insC
ENST00000482025.5:n.1873+78_1873+79insC
ENST00000482343.5:n.1471+78_1471+79insC
ENST00000490310.1:n.857_858insC
ENST00000492824.5:n.2067+78_2067+79insC
ENST00000495054.1:n.690+78_690+79insC
NM_001145862.1:c.1647+78_1647+79insC	NP_001139334.1:n.1647+78_1647+79insC
NM_181873.3:c.1431+78_1431+79insC	NP_870988.2:n.1431+78_1431+79insC
XM_006711135.1:c.1539+78_1539+79insC	XP_006711198.1:n.1539+78_1539+79insC
XM_006711136.2:c.1431+78_1431+79insC	XP_006711199.1:n.1431+78_1431+79insC
XM_006711137.1:c.1431+78_1431+79insC	XP_006711200.1:n.1431+78_1431+79insC
XM_011509098.1:c.1563+78_1563+79insC	XP_011507400.1:n.1563+78_1563+79insC
XM_011509099.1:c.*683_*684insC	XP_011507401.1:n.*683_*684insC
XR_426759.2:n.1838+78_1838+79insC
XR_426760.2:n.1744+78_1744+79insC
XM_011509099.3:c.*683_*684insC	XP_011507401.1:n.*683_*684insC
XM_024452577.1:c.1563+78_1563+79insC	XP_024308345.1:n.1563+78_1563+79insC
XM_024452578.1:c.1539+78_1539+79insC	XP_024308346.1:n.1539+78_1539+79insC
XR_002959043.1:n.1860+78_1860+79insC
XR_002959062.1:n.1976+78_1976+79insC
XR_002959066.1:n.1678+78_1678+79insC
XR_002959067.1:n.3197+78_3197+79insC
XR_426760.4:n.1766+78_1766+79insC
NM_001145862.2:c.1647+78_1647+79insC MANE Select	NP_001139334.1:n.1647+78_1647+79insC