Canonical Allele Identifier: CA408232785
Gene: MKKS HGNC NCBI

Linked Data

dbSNP Id: rs1449958697

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412931A>G , CM000682.2:g.10412931A>G GRCh38
NC_000020.10:g.10393579A>G , CM000682.1:g.10393579A>G GRCh37
NC_000020.9:g.10341579A>G NCBI36
NG_009109.1:g.26288T>C
NG_009109.2:g.26288T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.584T>C ENSP00000498849.1:p.Ile195Thr
ENST00000652676.1:n.459-231T>C
ENST00000347364.7:c.584T>C MANE Select ENSP00000246062.4:p.Ile195Thr
ENST00000399054.6:c.584T>C ENSP00000382008.2:p.Ile195Thr
NM_018848.3:c.584T>C NP_061336.1:p.Ile195Thr
NM_170784.2:c.584T>C NP_740754.1:p.Ile195Thr
NR_072977.1:n.364-4128T>C
NR_072977.2:n.347-4128T>C
NM_170784.3:c.584T>C MANE Select NP_740754.1:p.Ile195Thr