Canonical Allele Identifier: CA1627395151
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49457792G= , CM000668.2:g.49457792G= GRCh38
NC_000006.11:g.49425505G= , CM000668.1:g.49425505G= GRCh37
NC_000006.10:g.49533464G= NCBI36
NG_007100.1:g.10348C=

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.652C= MANE Select ENSP00000274813.3:p.Gln218=
ENST00000274813.3:c.652C= ENSP00000274813.3:p.Gln218=
NM_000255.3:c.652C= NP_000246.2:p.Gln218=
XM_005249143.2:c.652C= XP_005249200.1:p.Gln218=
XM_005249143.3:c.652C= XP_005249200.1:p.Gln218=
NM_000255.4:c.652C= MANE Select NP_000246.2:p.Gln218=