Canonical Allele Identifier: CA1627395257

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49457825C= , CM000668.2:g.49457825C=	GRCh38
NC_000006.11:g.49425538C= , CM000668.1:g.49425538C=	GRCh37
NC_000006.10:g.49533497C=	NCBI36
NG_007100.1:g.10315G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000274813.4:c.619G= MANE Select	ENSP00000274813.3:p.Gly207=
ENST00000274813.3:c.619G=	ENSP00000274813.3:p.Gly207=
NM_000255.3:c.619G=	NP_000246.2:p.Gly207=
XM_005249143.2:c.619G=	XP_005249200.1:p.Gly207=
XM_005249143.3:c.619G=	XP_005249200.1:p.Gly207=
NM_000255.4:c.619G= MANE Select	NP_000246.2:p.Gly207=