Canonical Allele Identifier: CA2573897944
Gene: MTMR11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149930281G>T , CM000663.2:g.149930281G>T GRCh38
NC_000001.10:g.149902173G>T , CM000663.1:g.149902173G>T GRCh37
NC_000001.9:g.148168797G>T NCBI36
NG_032777.1:g.2972C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000439741.4:c.1647+84C>A MANE Select ENSP00000391668.2:n.1647+84C>A
ENST00000369140.7:c.1431+84C>A ENSP00000358136.3:n.1431+84C>A
ENST00000439741.2:c.1647+84C>A ENSP00000391668.2:n.1647+84C>A
ENST00000466496.5:n.967+84C>A
ENST00000482025.5:n.1873+84C>A
ENST00000482343.5:n.1471+84C>A
ENST00000490310.1:n.863C>A
ENST00000492824.5:n.2067+84C>A
ENST00000495054.1:n.690+84C>A
NM_001145862.1:c.1647+84C>A NP_001139334.1:n.1647+84C>A
NM_181873.3:c.1431+84C>A NP_870988.2:n.1431+84C>A
XM_006711135.1:c.1539+84C>A XP_006711198.1:n.1539+84C>A
XM_006711136.2:c.1431+84C>A XP_006711199.1:n.1431+84C>A
XM_006711137.1:c.1431+84C>A XP_006711200.1:n.1431+84C>A
XM_011509098.1:c.1563+84C>A XP_011507400.1:n.1563+84C>A
XM_011509099.1:c.*689C>A XP_011507401.1:n.*689C>A
XR_426759.2:n.1838+84C>A
XR_426760.2:n.1744+84C>A
XM_011509099.3:c.*689C>A XP_011507401.1:n.*689C>A
XM_024452577.1:c.1563+84C>A XP_024308345.1:n.1563+84C>A
XM_024452578.1:c.1539+84C>A XP_024308346.1:n.1539+84C>A
XR_002959043.1:n.1860+84C>A
XR_002959062.1:n.1976+84C>A
XR_002959066.1:n.1678+84C>A
XR_002959067.1:n.3197+84C>A
XR_426760.4:n.1766+84C>A
NM_001145862.2:c.1647+84C>A MANE Select NP_001139334.1:n.1647+84C>A