Canonical Allele Identifier: CA1072161
Gene: MTMR11 HGNC NCBI

Linked Data

dbSNP Id: rs11205303

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149934520T>C , CM000663.2:g.149934520T>C GRCh38
NC_000001.10:g.149906413T>C , CM000663.1:g.149906413T>C GRCh37
NC_000001.9:g.148173037T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439741.4:c.475A>G MANE Select ENSP00000391668.2:p.Met159Val
ENST00000369140.7:c.259A>G ENSP00000358136.3:p.Met87Val
ENST00000439741.2:c.475A>G ENSP00000391668.2:p.Met159Val
ENST00000466496.5:n.402A>G
ENST00000479272.1:n.338A>G
ENST00000482025.5:n.712A>G
ENST00000482343.5:n.662A>G
ENST00000492824.5:n.662A>G
NM_001145862.1:c.475A>G NP_001139334.1:p.Met159Val
NM_181873.3:c.259A>G NP_870988.2:p.Met87Val
XM_006711135.1:c.367A>G XP_006711198.1:p.Met123Val
XM_006711136.2:c.259A>G XP_006711199.1:p.Met87Val
XM_006711137.1:c.259A>G XP_006711200.1:p.Met87Val
XM_011509098.1:c.391A>G XP_011507400.1:p.Met131Val
XM_011509099.1:c.475A>G XP_011507401.1:p.Met159Val
XM_011509100.1:c.475A>G XP_011507402.1:p.Met159Val
XR_426759.2:n.619A>G
XR_426760.2:n.619A>G
XM_011509099.3:c.475A>G XP_011507401.1:p.Met159Val
XM_024452577.1:c.391A>G XP_024308345.1:p.Met131Val
XM_024452578.1:c.367A>G XP_024308346.1:p.Met123Val
XM_024452592.1:c.475A>G XP_024308360.1:p.Met159Val
XR_002959043.1:n.641A>G
XR_002959062.1:n.851A>G
XR_002959066.1:n.553A>G
XR_002959067.1:n.2072A>G
XR_426760.4:n.641A>G
NM_001145862.2:c.475A>G MANE Select NP_001139334.1:p.Met159Val