Canonical Allele Identifier: CA1627397166
Gene: MMUT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.49459408T= , CM000668.2:g.49459408T= GRCh38
NC_000006.11:g.49427121T= , CM000668.1:g.49427121T= GRCh37
NC_000006.10:g.49535080T= NCBI36
NG_007100.1:g.8732A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000274813.4:c.59A= MANE Select ENSP00000274813.3:p.Lys20=
ENST00000274813.3:c.59A= ENSP00000274813.3:p.Lys20=
NM_000255.3:c.59A= NP_000246.2:p.Lys20=
XM_005249143.2:c.59A= XP_005249200.1:p.Lys20=
XM_005249143.3:c.59A= XP_005249200.1:p.Lys20=
NM_000255.4:c.59A= MANE Select NP_000246.2:p.Lys20=