Canonical Allele Identifier: CA1627389345

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49451634A= , CM000668.2:g.49451634A=	GRCh38
NC_000006.11:g.49419347A= , CM000668.1:g.49419347A=	GRCh37
NC_000006.10:g.49527306A=	NCBI36
NG_007100.1:g.16506T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.1164T= MANE Select	ENSP00000274813.3:p.Asn388=
ENST00000274813.3:c.1164T=	ENSP00000274813.3:p.Asn388=
NM_000255.3:c.1164T=	NP_000246.2:p.Asn388=
XM_005249143.2:c.1164T=	XP_005249200.1:p.Asn388=
XM_005249143.3:c.1164T=	XP_005249200.1:p.Asn388=
NM_000255.4:c.1164T= MANE Select	NP_000246.2:p.Asn388=