Canonical Allele Identifier: CA2349780886
Gene: MKKS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412959T= , CM000682.2:g.10412959T= GRCh38
NC_000020.10:g.10393607T= , CM000682.1:g.10393607T= GRCh37
NC_000020.9:g.10341607T= NCBI36
NG_009109.1:g.26260A=
NG_009109.2:g.26260A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.556A= ENSP00000498849.1:p.Ile186=
ENST00000652676.1:n.459-259A=
ENST00000347364.7:c.556A= MANE Select ENSP00000246062.4:p.Ile186=
ENST00000399054.6:c.556A= ENSP00000382008.2:p.Ile186=
NM_018848.3:c.556A= NP_061336.1:p.Ile186=
NM_170784.2:c.556A= NP_740754.1:p.Ile186=
NR_072977.1:n.364-4156A=
NR_072977.2:n.347-4156A=
NM_170784.3:c.556A= MANE Select NP_740754.1:p.Ile186=