Canonical Allele Identifier: CA1627388079
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49448789C= , CM000668.2:g.49448789C= GRCh38
NC_000006.11:g.49416502C= , CM000668.1:g.49416502C= GRCh37
NC_000006.10:g.49524461C= NCBI36
NG_007100.1:g.19351G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1444+27G= MANE Select ENSP00000274813.3:n.1444+27G=
ENST00000274813.3:c.1444+27G= ENSP00000274813.3:n.1444+27G=
NM_000255.3:c.1444+27G= NP_000246.2:n.1444+27G=
XM_005249143.2:c.1444+27G= XP_005249200.1:n.1444+27G=
XM_005249143.3:c.1444+27G= XP_005249200.1:n.1444+27G=
NM_000255.4:c.1444+27G= MANE Select NP_000246.2:n.1444+27G=