Canonical Allele Identifier: CA509814932
Gene: MKKS HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.10393266T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412618T>A , CM000682.2:g.10412618T>A GRCh38
NC_000020.10:g.10393266T>A , CM000682.1:g.10393266T>A GRCh37
NC_000020.9:g.10341266T>A NCBI36
NG_009109.1:g.26601A>T
NG_009109.2:g.26601A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.897A>T ENSP00000498849.1:p.Pro299=
ENST00000652676.1:n.541A>T
ENST00000347364.7:c.897A>T MANE Select ENSP00000246062.4:p.Pro299=
ENST00000399054.6:c.897A>T ENSP00000382008.2:p.Pro299=
NM_018848.3:c.897A>T NP_061336.1:p.Pro299=
NM_170784.2:c.897A>T NP_740754.1:p.Pro299=
NR_072977.1:n.364-3815A>T
NR_072977.2:n.347-3815A>T
NM_170784.3:c.897A>T MANE Select NP_740754.1:p.Pro299=