Canonical Allele Identifier: CA1627396519

Gene: MMUT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.49459108T= , CM000668.2:g.49459108T=	GRCh38
NC_000006.11:g.49426821T= , CM000668.1:g.49426821T=	GRCh37
NC_000006.10:g.49534780T=	NCBI36
NG_007100.1:g.9032A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000274813.4:c.359A= MANE Select	ENSP00000274813.3:p.Asn120=
ENST00000274813.3:c.359A=	ENSP00000274813.3:p.Asn120=
NM_000255.3:c.359A=	NP_000246.2:p.Asn120=
XM_005249143.2:c.359A=	XP_005249200.1:p.Asn120=
XM_005249143.3:c.359A=	XP_005249200.1:p.Asn120=
NM_000255.4:c.359A= MANE Select	NP_000246.2:p.Asn120=