Canonical Allele Identifier: CA342284402
Gene: MTMR11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149930378A>T , CM000663.2:g.149930378A>T GRCh38
NC_000001.10:g.149902270A>T , CM000663.1:g.149902270A>T GRCh37
NC_000001.9:g.148168894A>T NCBI36
NG_032777.1:g.2875T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000439741.4:c.1634T>A MANE Select ENSP00000391668.2:p.Leu545His
ENST00000369140.7:c.1418T>A ENSP00000358136.3:p.Leu473His
ENST00000439741.2:c.1634T>A ENSP00000391668.2:p.Leu545His
ENST00000466496.5:n.954T>A
ENST00000482025.5:n.1860T>A
ENST00000482343.5:n.1458T>A
ENST00000490310.1:n.766T>A
ENST00000492824.5:n.2054T>A
ENST00000495054.1:n.677T>A
NM_001145862.1:c.1634T>A NP_001139334.1:p.Leu545His
NM_181873.3:c.1418T>A NP_870988.2:p.Leu473His
XM_006711135.1:c.1526T>A XP_006711198.1:p.Leu509His
XM_006711136.2:c.1418T>A XP_006711199.1:p.Leu473His
XM_006711137.1:c.1418T>A XP_006711200.1:p.Leu473His
XM_011509098.1:c.1550T>A XP_011507400.1:p.Leu517His
XM_011509099.1:c.*592T>A XP_011507401.1:n.*592T>A
XR_426759.2:n.1825T>A
XR_426760.2:n.1731T>A
XM_011509099.3:c.*592T>A XP_011507401.1:n.*592T>A
XM_024452577.1:c.1550T>A XP_024308345.1:p.Leu517His
XM_024452578.1:c.1526T>A XP_024308346.1:p.Leu509His
XR_002959043.1:n.1847T>A
XR_002959062.1:n.1963T>A
XR_002959066.1:n.1665T>A
XR_002959067.1:n.3184T>A
XR_426760.4:n.1753T>A
NM_001145862.2:c.1634T>A MANE Select NP_001139334.1:p.Leu545His