Canonical Allele Identifier: CA2267730819

Gene: MTMR4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58506716C= , CM000679.2:g.58506716C=	GRCh38
NC_000017.10:g.56584077C= , CM000679.1:g.56584077C=	GRCh37
NC_000017.9:g.53939076C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682306.1:c.1033+27G= MANE Select	ENSP00000507664.1:n.1033+27G=
ENST00000323456.9:c.991+27G=	ENSP00000325285.5:n.991+27G=
ENST00000579925.5:c.991+27G=	ENSP00000464067.1:n.991+27G=
NM_004687.4:c.991+27G=	NP_004678.3:n.991+27G=
XM_005257784.2:c.1033+27G=	XP_005257841.1:n.1033+27G=
XM_005257785.3:c.1003+27G=	XP_005257842.1:n.1003+27G=
XM_005257786.3:c.991+27G=	XP_005257843.1:n.991+27G=
XM_006722168.2:c.991+27G=	XP_006722231.1:n.991+27G=
XM_011525460.1:c.1003+27G=	XP_011523762.1:n.1003+27G=
XM_005257785.5:c.1003+27G=	XP_005257842.1:n.1003+27G=
XM_005257786.5:c.991+27G=	XP_005257843.1:n.991+27G=
XM_006722168.4:c.991+27G=	XP_006722231.1:n.991+27G=
XM_011525460.3:c.1003+27G=	XP_011523762.1:n.1003+27G=
NM_004687.5:c.991+27G=	NP_004678.3:n.991+27G=
NM_001378066.1:c.1003+27G=	NP_001364995.1:n.1003+27G=
NM_001378067.1:c.1033+27G= MANE Select	NP_001364996.1:n.1033+27G=