Canonical Allele Identifier: CA2349780884
Gene: MKKS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412945A= , CM000682.2:g.10412945A= GRCh38
NC_000020.10:g.10393593A= , CM000682.1:g.10393593A= GRCh37
NC_000020.9:g.10341593A= NCBI36
NG_009109.1:g.26274T=
NG_009109.2:g.26274T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.570T= ENSP00000498849.1:p.Ala190=
ENST00000652676.1:n.459-245T=
ENST00000347364.7:c.570T= MANE Select ENSP00000246062.4:p.Ala190=
ENST00000399054.6:c.570T= ENSP00000382008.2:p.Ala190=
NM_018848.3:c.570T= NP_061336.1:p.Ala190=
NM_170784.2:c.570T= NP_740754.1:p.Ala190=
NR_072977.1:n.364-4142T=
NR_072977.2:n.347-4142T=
NM_170784.3:c.570T= MANE Select NP_740754.1:p.Ala190=