Canonical Allele Identifier: CA400362739
Gene: MTMR4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58506781A>T , CM000679.2:g.58506781A>T GRCh38
NC_000017.10:g.56584142A>T , CM000679.1:g.56584142A>T GRCh37
NC_000017.9:g.53939141A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682306.1:c.995T>A MANE Select ENSP00000507664.1:p.Val332Glu
ENST00000323456.9:c.953T>A ENSP00000325285.5:p.Val318Glu
ENST00000579925.5:c.953T>A ENSP00000464067.1:p.Val318Glu
NM_004687.4:c.953T>A NP_004678.3:p.Val318Glu
XM_005257784.2:c.995T>A XP_005257841.1:p.Val332Glu
XM_005257785.3:c.965T>A XP_005257842.1:p.Val322Glu
XM_005257786.3:c.953T>A XP_005257843.1:p.Val318Glu
XM_006722168.2:c.953T>A XP_006722231.1:p.Val318Glu
XM_011525460.1:c.965T>A XP_011523762.1:p.Val322Glu
XM_005257785.5:c.965T>A XP_005257842.1:p.Val322Glu
XM_005257786.5:c.953T>A XP_005257843.1:p.Val318Glu
XM_006722168.4:c.953T>A XP_006722231.1:p.Val318Glu
XM_011525460.3:c.965T>A XP_011523762.1:p.Val322Glu
NM_004687.5:c.953T>A NP_004678.3:p.Val318Glu
NM_001378066.1:c.965T>A NP_001364995.1:p.Val322Glu
NM_001378067.1:c.995T>A MANE Select NP_001364996.1:p.Val332Glu