Canonical Allele Identifier: CA2349780890
Gene: MKKS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412970A= , CM000682.2:g.10412970A= GRCh38
NC_000020.10:g.10393618A= , CM000682.1:g.10393618A= GRCh37
NC_000020.9:g.10341618A= NCBI36
NG_009109.1:g.26249T=
NG_009109.2:g.26249T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.545T= ENSP00000498849.1:p.Phe182=
ENST00000652676.1:n.459-270T=
ENST00000347364.7:c.545T= MANE Select ENSP00000246062.4:p.Phe182=
ENST00000399054.6:c.545T= ENSP00000382008.2:p.Phe182=
NM_018848.3:c.545T= NP_061336.1:p.Phe182=
NM_170784.2:c.545T= NP_740754.1:p.Phe182=
NR_072977.1:n.364-4167T=
NR_072977.2:n.347-4167T=
NM_170784.3:c.545T= MANE Select NP_740754.1:p.Phe182=