Canonical Allele Identifier: CA1627387657
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447790T= , CM000668.2:g.49447790T= GRCh38
NC_000006.11:g.49415503T= , CM000668.1:g.49415503T= GRCh37
NC_000006.10:g.49523462T= NCBI36
NG_007100.1:g.20350A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1445-5A= MANE Select ENSP00000274813.3:n.1445-5A=
ENST00000274813.3:c.1445-5A= ENSP00000274813.3:n.1445-5A=
NM_000255.3:c.1445-5A= NP_000246.2:n.1445-5A=
XM_005249143.2:c.1445-5A= XP_005249200.1:n.1445-5A=
XM_005249143.3:c.1445-5A= XP_005249200.1:n.1445-5A=
NM_000255.4:c.1445-5A= MANE Select NP_000246.2:n.1445-5A=