Canonical Allele Identifier: CA1763808829
Gene: MTMR9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11319901G= , CM000670.2:g.11319901G= GRCh38
NC_000008.10:g.11177410G= , CM000670.1:g.11177410G= GRCh37
NC_000008.9:g.11214820G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000221086.8:c.1486+63G= MANE Select ENSP00000221086.3:n.1486+63G=
ENST00000221086.7:c.1486+63G= ENSP00000221086.3:n.1486+63G=
ENST00000526292.1:c.1231+63G= ENSP00000433239.1:n.1231+63G=
ENST00000530200.1:c.*1232+63G= ENSP00000436046.1:n.*1232+63G=
NM_015458.3:c.1486+63G= NP_056273.2:n.1486+63G=
XM_011543830.1:c.1165+63G= XP_011542132.1:n.1165+63G=
XM_011543831.1:c.898+63G= XP_011542133.1:n.898+63G=
XM_011543830.3:c.1165+63G= XP_011542132.1:n.1165+63G=
XM_011543831.2:c.898+63G= XP_011542133.1:n.898+63G=
NM_015458.4:c.1486+63G= MANE Select NP_056273.2:n.1486+63G=