Canonical Allele Identifier: CA2267730828

Gene: MTMR4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.58506754C= , CM000679.2:g.58506754C=	GRCh38
NC_000017.10:g.56584115C= , CM000679.1:g.56584115C=	GRCh37
NC_000017.9:g.53939114C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682306.1:c.1022G= MANE Select	ENSP00000507664.1:p.Cys341=
ENST00000323456.9:c.980G=	ENSP00000325285.5:p.Cys327=
ENST00000579925.5:c.980G=	ENSP00000464067.1:p.Cys327=
NM_004687.4:c.980G=	NP_004678.3:p.Cys327=
XM_005257784.2:c.1022G=	XP_005257841.1:p.Cys341=
XM_005257785.3:c.992G=	XP_005257842.1:p.Cys331=
XM_005257786.3:c.980G=	XP_005257843.1:p.Cys327=
XM_006722168.2:c.980G=	XP_006722231.1:p.Cys327=
XM_011525460.1:c.992G=	XP_011523762.1:p.Cys331=
XM_005257785.5:c.992G=	XP_005257842.1:p.Cys331=
XM_005257786.5:c.980G=	XP_005257843.1:p.Cys327=
XM_006722168.4:c.980G=	XP_006722231.1:p.Cys327=
XM_011525460.3:c.992G=	XP_011523762.1:p.Cys331=
NM_004687.5:c.980G=	NP_004678.3:p.Cys327=
NM_001378066.1:c.992G=	NP_001364995.1:p.Cys331=
NM_001378067.1:c.1022G= MANE Select	NP_001364996.1:p.Cys341=