Canonical Allele Identifier: CA2349780952
Gene: MKKS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10413082T= , CM000682.2:g.10413082T= GRCh38
NC_000020.10:g.10393730T= , CM000682.1:g.10393730T= GRCh37
NC_000020.9:g.10341730T= NCBI36
NG_009109.1:g.26137A=
NG_009109.2:g.26137A=

Transcript Alleles

HGVS Amino-acid change
ENST00000651692.1:c.433A= ENSP00000498849.1:p.Ser145=
ENST00000652676.1:n.459-382A=
ENST00000347364.7:c.433A= MANE Select ENSP00000246062.4:p.Ser145=
ENST00000399054.6:c.433A= ENSP00000382008.2:p.Ser145=
NM_018848.3:c.433A= NP_061336.1:p.Ser145=
NM_170784.2:c.433A= NP_740754.1:p.Ser145=
NR_072977.1:n.364-4279A=
NR_072977.2:n.347-4279A=
NM_170784.3:c.433A= MANE Select NP_740754.1:p.Ser145=