Canonical Allele Identifier: CA1627387614
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49447694G= , CM000668.2:g.49447694G= GRCh38
NC_000006.11:g.49415407G= , CM000668.1:g.49415407G= GRCh37
NC_000006.10:g.49523366G= NCBI36
NG_007100.1:g.20446C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.1536C= MANE Select ENSP00000274813.3:p.Asn512=
ENST00000274813.3:c.1536C= ENSP00000274813.3:p.Asn512=
NM_000255.3:c.1536C= NP_000246.2:p.Asn512=
XM_005249143.2:c.1536C= XP_005249200.1:p.Asn512=
XM_005249143.3:c.1536C= XP_005249200.1:p.Asn512=
NM_000255.4:c.1536C= MANE Select NP_000246.2:p.Asn512=