Canonical Allele Identifier: CA1627392095

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49457757A= , CM000668.2:g.49457757A=	GRCh38
NC_000006.11:g.49425470A= , CM000668.1:g.49425470A=	GRCh37
NC_000006.10:g.49533429A=	NCBI36
NG_007100.1:g.10383T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.687T= MANE Select	ENSP00000274813.3:p.Asn229=
ENST00000274813.3:c.687T=	ENSP00000274813.3:p.Asn229=
NM_000255.3:c.687T=	NP_000246.2:p.Asn229=
XM_005249143.2:c.687T=	XP_005249200.1:p.Asn229=
XM_005249143.3:c.687T=	XP_005249200.1:p.Asn229=
NM_000255.4:c.687T= MANE Select	NP_000246.2:p.Asn229=