Canonical Allele Identifier: CA1627396592
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459144C= , CM000668.2:g.49459144C= GRCh38
NC_000006.11:g.49426857C= , CM000668.1:g.49426857C= GRCh37
NC_000006.10:g.49534816C= NCBI36
NG_007100.1:g.8996G=

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.323G= MANE Select ENSP00000274813.3:p.Arg108=
ENST00000274813.3:c.323G= ENSP00000274813.3:p.Arg108=
NM_000255.3:c.323G= NP_000246.2:p.Arg108=
XM_005249143.2:c.323G= XP_005249200.1:p.Arg108=
XM_005249143.3:c.323G= XP_005249200.1:p.Arg108=
NM_000255.4:c.323G= MANE Select NP_000246.2:p.Arg108=