Canonical Allele Identifier: CA2647759210
Gene: MTMR11 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.149930301T>C , CM000663.2:g.149930301T>C GRCh38
NC_000001.10:g.149902193T>C , CM000663.1:g.149902193T>C GRCh37
NC_000001.9:g.148168817T>C NCBI36
NG_032777.1:g.2952A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000439741.4:c.1647+64A>G MANE Select ENSP00000391668.2:n.1647+64A>G
ENST00000369140.7:c.1431+64A>G ENSP00000358136.3:n.1431+64A>G
ENST00000439741.2:c.1647+64A>G ENSP00000391668.2:n.1647+64A>G
ENST00000466496.5:n.967+64A>G
ENST00000482025.5:n.1873+64A>G
ENST00000482343.5:n.1471+64A>G
ENST00000490310.1:n.843A>G
ENST00000492824.5:n.2067+64A>G
ENST00000495054.1:n.690+64A>G
NM_001145862.1:c.1647+64A>G NP_001139334.1:n.1647+64A>G
NM_181873.3:c.1431+64A>G NP_870988.2:n.1431+64A>G
XM_006711135.1:c.1539+64A>G XP_006711198.1:n.1539+64A>G
XM_006711136.2:c.1431+64A>G XP_006711199.1:n.1431+64A>G
XM_006711137.1:c.1431+64A>G XP_006711200.1:n.1431+64A>G
XM_011509098.1:c.1563+64A>G XP_011507400.1:n.1563+64A>G
XM_011509099.1:c.*669A>G XP_011507401.1:n.*669A>G
XR_426759.2:n.1838+64A>G
XR_426760.2:n.1744+64A>G
XM_011509099.3:c.*669A>G XP_011507401.1:n.*669A>G
XM_024452577.1:c.1563+64A>G XP_024308345.1:n.1563+64A>G
XM_024452578.1:c.1539+64A>G XP_024308346.1:n.1539+64A>G
XR_002959043.1:n.1860+64A>G
XR_002959062.1:n.1976+64A>G
XR_002959066.1:n.1678+64A>G
XR_002959067.1:n.3197+64A>G
XR_426760.4:n.1766+64A>G
NM_001145862.2:c.1647+64A>G MANE Select NP_001139334.1:n.1647+64A>G