Canonical Allele Identifier: CA1627387676
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447839G= , CM000668.2:g.49447839G= GRCh38
NC_000006.11:g.49415552G= , CM000668.1:g.49415552G= GRCh37
NC_000006.10:g.49523511G= NCBI36
NG_007100.1:g.20301C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1445-54C= MANE Select ENSP00000274813.3:n.1445-54C=
ENST00000274813.3:c.1445-54C= ENSP00000274813.3:n.1445-54C=
NM_000255.3:c.1445-54C= NP_000246.2:n.1445-54C=
XM_005249143.2:c.1445-54C= XP_005249200.1:n.1445-54C=
XM_005249143.3:c.1445-54C= XP_005249200.1:n.1445-54C=
NM_000255.4:c.1445-54C= MANE Select NP_000246.2:n.1445-54C=