Canonical Allele Identifier: CA1627396820

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459231A= , CM000668.2:g.49459231A=	GRCh38
NC_000006.11:g.49426944A= , CM000668.1:g.49426944A=	GRCh37
NC_000006.10:g.49534903A=	NCBI36
NG_007100.1:g.8909T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.236T= MANE Select	ENSP00000274813.3:p.Met79=
ENST00000274813.3:c.236T=	ENSP00000274813.3:p.Met79=
NM_000255.3:c.236T=	NP_000246.2:p.Met79=
XM_005249143.2:c.236T=	XP_005249200.1:p.Met79=
XM_005249143.3:c.236T=	XP_005249200.1:p.Met79=
NM_000255.4:c.236T= MANE Select	NP_000246.2:p.Met79=