Canonical Allele Identifier: CA2267730832
Gene: MTMR4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.58506765C= , CM000679.2:g.58506765C= GRCh38
NC_000017.10:g.56584126C= , CM000679.1:g.56584126C= GRCh37
NC_000017.9:g.53939125C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682306.1:c.1011G= MANE Select ENSP00000507664.1:p.Lys337=
ENST00000323456.9:c.969G= ENSP00000325285.5:p.Lys323=
ENST00000579925.5:c.969G= ENSP00000464067.1:p.Lys323=
NM_004687.4:c.969G= NP_004678.3:p.Lys323=
XM_005257784.2:c.1011G= XP_005257841.1:p.Lys337=
XM_005257785.3:c.981G= XP_005257842.1:p.Lys327=
XM_005257786.3:c.969G= XP_005257843.1:p.Lys323=
XM_006722168.2:c.969G= XP_006722231.1:p.Lys323=
XM_011525460.1:c.981G= XP_011523762.1:p.Lys327=
XM_005257785.5:c.981G= XP_005257842.1:p.Lys327=
XM_005257786.5:c.969G= XP_005257843.1:p.Lys323=
XM_006722168.4:c.969G= XP_006722231.1:p.Lys323=
XM_011525460.3:c.981G= XP_011523762.1:p.Lys327=
NM_004687.5:c.969G= NP_004678.3:p.Lys323=
NM_001378066.1:c.981G= NP_001364995.1:p.Lys327=
NM_001378067.1:c.1011G= MANE Select NP_001364996.1:p.Lys337=