Canonical Allele Identifier: CA1627395701

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49458158C= , CM000668.2:g.49458158C=	GRCh38
NC_000006.11:g.49425871C= , CM000668.1:g.49425871C=	GRCh37
NC_000006.10:g.49533830C=	NCBI36
NG_007100.1:g.9982G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.386-100G= MANE Select	ENSP00000274813.3:n.386-100G=
ENST00000274813.3:c.386-100G=	ENSP00000274813.3:n.386-100G=
NM_000255.3:c.386-100G=	NP_000246.2:n.386-100G=
XM_005249143.2:c.386-100G=	XP_005249200.1:n.386-100G=
XM_005249143.3:c.386-100G=	XP_005249200.1:n.386-100G=
NM_000255.4:c.386-100G= MANE Select	NP_000246.2:n.386-100G=