Canonical Allele Identifier: CA1627373946
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49431730A= , CM000668.2:g.49431730A= GRCh38
NC_000006.11:g.49399443A= , CM000668.1:g.49399443A= GRCh37
NC_000006.10:g.49507402A= NCBI36
NG_007100.1:g.36410T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.2251T= MANE Select ENSP00000274813.3:p.Ter751=
ENST00000274813.3:c.2251T= ENSP00000274813.3:p.Ter751=
NM_000255.3:c.2251T= NP_000246.2:p.Ter751=
XM_005249143.2:c.2251T= XP_005249200.1:p.Ter751=
XM_005249143.3:c.2251T= XP_005249200.1:p.Ter751=
NM_000255.4:c.2251T= MANE Select NP_000246.2:p.Ter751=