Canonical Allele Identifier: CA2349780878
Gene: MKKS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412931A= , CM000682.2:g.10412931A= GRCh38
NC_000020.10:g.10393579A= , CM000682.1:g.10393579A= GRCh37
NC_000020.9:g.10341579A= NCBI36
NG_009109.1:g.26288T=
NG_009109.2:g.26288T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.584T= ENSP00000498849.1:p.Ile195=
ENST00000652676.1:n.459-231T=
ENST00000347364.7:c.584T= MANE Select ENSP00000246062.4:p.Ile195=
ENST00000399054.6:c.584T= ENSP00000382008.2:p.Ile195=
NM_018848.3:c.584T= NP_061336.1:p.Ile195=
NM_170784.2:c.584T= NP_740754.1:p.Ile195=
NR_072977.1:n.364-4128T=
NR_072977.2:n.347-4128T=
NM_170784.3:c.584T= MANE Select NP_740754.1:p.Ile195=