Canonical Allele Identifier: CA1627397215

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459416C= , CM000668.2:g.49459416C=	GRCh38
NC_000006.11:g.49427129C= , CM000668.1:g.49427129C=	GRCh37
NC_000006.10:g.49535088C=	NCBI36
NG_007100.1:g.8724G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.51G= MANE Select	ENSP00000274813.3:p.Arg17=
ENST00000274813.3:c.51G=	ENSP00000274813.3:p.Arg17=
NM_000255.3:c.51G=	NP_000246.2:p.Arg17=
XM_005249143.2:c.51G=	XP_005249200.1:p.Arg17=
XM_005249143.3:c.51G=	XP_005249200.1:p.Arg17=
NM_000255.4:c.51G= MANE Select	NP_000246.2:p.Arg17=