Canonical Allele Identifier: CA2349780859
Gene: MKKS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412894T= , CM000682.2:g.10412894T= GRCh38
NC_000020.10:g.10393542T= , CM000682.1:g.10393542T= GRCh37
NC_000020.9:g.10341542T= NCBI36
NG_009109.1:g.26325A=
NG_009109.2:g.26325A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.621A= ENSP00000498849.1:p.Gln207=
ENST00000652676.1:n.459-194A=
ENST00000347364.7:c.621A= MANE Select ENSP00000246062.4:p.Gln207=
ENST00000399054.6:c.621A= ENSP00000382008.2:p.Gln207=
NM_018848.3:c.621A= NP_061336.1:p.Gln207=
NM_170784.2:c.621A= NP_740754.1:p.Gln207=
NR_072977.1:n.364-4091A=
NR_072977.2:n.347-4091A=
NM_170784.3:c.621A= MANE Select NP_740754.1:p.Gln207=