Canonical Allele Identifier: CA408233112
Gene: MKKS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10413080A>C , CM000682.2:g.10413080A>C GRCh38
NC_000020.10:g.10393728A>C , CM000682.1:g.10393728A>C GRCh37
NC_000020.9:g.10341728A>C NCBI36
NG_009109.1:g.26139T>G
NG_009109.2:g.26139T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000651692.1:c.435T>G ENSP00000498849.1:p.Ser145Arg
ENST00000652676.1:n.459-380T>G
ENST00000347364.7:c.435T>G MANE Select ENSP00000246062.4:p.Ser145Arg
ENST00000399054.6:c.435T>G ENSP00000382008.2:p.Ser145Arg
NM_018848.3:c.435T>G NP_061336.1:p.Ser145Arg
NM_170784.2:c.435T>G NP_740754.1:p.Ser145Arg
NR_072977.1:n.364-4277T>G
NR_072977.2:n.347-4277T>G
NM_170784.3:c.435T>G MANE Select NP_740754.1:p.Ser145Arg