Canonical Allele Identifier: CA1627396980

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459289T= , CM000668.2:g.49459289T=	GRCh38
NC_000006.11:g.49427002T= , CM000668.1:g.49427002T=	GRCh37
NC_000006.10:g.49534961T=	NCBI36
NG_007100.1:g.8851A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.178A= MANE Select	ENSP00000274813.3:p.Ile60=
ENST00000274813.3:c.178A=	ENSP00000274813.3:p.Ile60=
NM_000255.3:c.178A=	NP_000246.2:p.Ile60=
XM_005249143.2:c.178A=	XP_005249200.1:p.Ile60=
XM_005249143.3:c.178A=	XP_005249200.1:p.Ile60=
NM_000255.4:c.178A= MANE Select	NP_000246.2:p.Ile60=