Canonical Allele Identifier: CA2349780958
Gene: MKKS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10413089C= , CM000682.2:g.10413089C= GRCh38
NC_000020.10:g.10393737C= , CM000682.1:g.10393737C= GRCh37
NC_000020.9:g.10341737C= NCBI36
NG_009109.1:g.26130G=
NG_009109.2:g.26130G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.426G= ENSP00000498849.1:p.Val142=
ENST00000652676.1:n.459-389G=
ENST00000347364.7:c.426G= MANE Select ENSP00000246062.4:p.Val142=
ENST00000399054.6:c.426G= ENSP00000382008.2:p.Val142=
NM_018848.3:c.426G= NP_061336.1:p.Val142=
NM_170784.2:c.426G= NP_740754.1:p.Val142=
NR_072977.1:n.364-4286G=
NR_072977.2:n.347-4286G=
NM_170784.3:c.426G= MANE Select NP_740754.1:p.Val142=