Canonical Allele Identifier: CA1627395322

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49457922A= , CM000668.2:g.49457922A=	GRCh38
NC_000006.11:g.49425635A= , CM000668.1:g.49425635A=	GRCh37
NC_000006.10:g.49533594A=	NCBI36
NG_007100.1:g.10218T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.522T= MANE Select	ENSP00000274813.3:p.Phe174=
ENST00000274813.3:c.522T=	ENSP00000274813.3:p.Phe174=
NM_000255.3:c.522T=	NP_000246.2:p.Phe174=
XM_005249143.2:c.522T=	XP_005249200.1:p.Phe174=
XM_005249143.3:c.522T=	XP_005249200.1:p.Phe174=
NM_000255.4:c.522T= MANE Select	NP_000246.2:p.Phe174=