Canonical Allele Identifier: CA1627392092
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49457754T= , CM000668.2:g.49457754T= GRCh38
NC_000006.11:g.49425467T= , CM000668.1:g.49425467T= GRCh37
NC_000006.10:g.49533426T= NCBI36
NG_007100.1:g.10386A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.690A= MANE Select ENSP00000274813.3:p.Thr230=
ENST00000274813.3:c.690A= ENSP00000274813.3:p.Thr230=
NM_000255.3:c.690A= NP_000246.2:p.Thr230=
XM_005249143.2:c.690A= XP_005249200.1:p.Thr230=
XM_005249143.3:c.690A= XP_005249200.1:p.Thr230=
NM_000255.4:c.690A= MANE Select NP_000246.2:p.Thr230=