Canonical Allele Identifier: CA509815246
Gene: MKKS HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.10393614C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412966C>T , CM000682.2:g.10412966C>T GRCh38
NC_000020.10:g.10393614C>T , CM000682.1:g.10393614C>T GRCh37
NC_000020.9:g.10341614C>T NCBI36
NG_009109.1:g.26253G>A
NG_009109.2:g.26253G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.549G>A ENSP00000498849.1:p.Leu183=
ENST00000652676.1:n.459-266G>A
ENST00000347364.7:c.549G>A MANE Select ENSP00000246062.4:p.Leu183=
ENST00000399054.6:c.549G>A ENSP00000382008.2:p.Leu183=
NM_018848.3:c.549G>A NP_061336.1:p.Leu183=
NM_170784.2:c.549G>A NP_740754.1:p.Leu183=
NR_072977.1:n.364-4163G>A
NR_072977.2:n.347-4163G>A
NM_170784.3:c.549G>A MANE Select NP_740754.1:p.Leu183=