Canonical Allele Identifier: CA1627387628

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49447729C= , CM000668.2:g.49447729C=	GRCh38
NC_000006.11:g.49415442C= , CM000668.1:g.49415442C=	GRCh37
NC_000006.10:g.49523401C=	NCBI36
NG_007100.1:g.20411G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1501G= MANE Select	ENSP00000274813.3:p.Glu501=
ENST00000274813.3:c.1501G=	ENSP00000274813.3:p.Glu501=
NM_000255.3:c.1501G=	NP_000246.2:p.Glu501=
XM_005249143.2:c.1501G=	XP_005249200.1:p.Glu501=
XM_005249143.3:c.1501G=	XP_005249200.1:p.Glu501=
NM_000255.4:c.1501G= MANE Select	NP_000246.2:p.Glu501=