Canonical Allele Identifier: CA2349780888
Gene: MKKS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412962T= , CM000682.2:g.10412962T= GRCh38
NC_000020.10:g.10393610T= , CM000682.1:g.10393610T= GRCh37
NC_000020.9:g.10341610T= NCBI36
NG_009109.1:g.26257A=
NG_009109.2:g.26257A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.553A= ENSP00000498849.1:p.Thr185=
ENST00000652676.1:n.459-262A=
ENST00000347364.7:c.553A= MANE Select ENSP00000246062.4:p.Thr185=
ENST00000399054.6:c.553A= ENSP00000382008.2:p.Thr185=
NM_018848.3:c.553A= NP_061336.1:p.Thr185=
NM_170784.2:c.553A= NP_740754.1:p.Thr185=
NR_072977.1:n.364-4159A=
NR_072977.2:n.347-4159A=
NM_170784.3:c.553A= MANE Select NP_740754.1:p.Thr185=