Canonical Allele Identifier: CA1627395125
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49457790T= , CM000668.2:g.49457790T= GRCh38
NC_000006.11:g.49425503T= , CM000668.1:g.49425503T= GRCh37
NC_000006.10:g.49533462T= NCBI36
NG_007100.1:g.10350A=

Transcript Alleles

HGVS Amino-acid change
ENST00000274813.4:c.654A= MANE Select ENSP00000274813.3:p.Gln218=
ENST00000274813.3:c.654A= ENSP00000274813.3:p.Gln218=
NM_000255.3:c.654A= NP_000246.2:p.Gln218=
XM_005249143.2:c.654A= XP_005249200.1:p.Gln218=
XM_005249143.3:c.654A= XP_005249200.1:p.Gln218=
NM_000255.4:c.654A= MANE Select NP_000246.2:p.Gln218=