Canonical Allele Identifier: CA1627395349

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49457937A= , CM000668.2:g.49457937A=	GRCh38
NC_000006.11:g.49425650A= , CM000668.1:g.49425650A=	GRCh37
NC_000006.10:g.49533609A=	NCBI36
NG_007100.1:g.10203T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000274813.4:c.507T= MANE Select	ENSP00000274813.3:p.Asp169=
ENST00000274813.3:c.507T=	ENSP00000274813.3:p.Asp169=
NM_000255.3:c.507T=	NP_000246.2:p.Asp169=
XM_005249143.2:c.507T=	XP_005249200.1:p.Asp169=
XM_005249143.3:c.507T=	XP_005249200.1:p.Asp169=
NM_000255.4:c.507T= MANE Select	NP_000246.2:p.Asp169=