Canonical Allele Identifier: CA1627396322

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459032A= , CM000668.2:g.49459032A=	GRCh38
NC_000006.11:g.49426745A= , CM000668.1:g.49426745A=	GRCh37
NC_000006.10:g.49534704A=	NCBI36
NG_007100.1:g.9108T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.385+50T= MANE Select	ENSP00000274813.3:n.385+50T=
ENST00000274813.3:c.385+50T=	ENSP00000274813.3:n.385+50T=
NM_000255.3:c.385+50T=	NP_000246.2:n.385+50T=
XM_005249143.2:c.385+50T=	XP_005249200.1:n.385+50T=
XM_005249143.3:c.385+50T=	XP_005249200.1:n.385+50T=
NM_000255.4:c.385+50T= MANE Select	NP_000246.2:n.385+50T=