Canonical Allele Identifier: CA2349780838
Gene: MKKS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412850_10412851delinsAT , CM000682.2:g.10412850_10412851delinsAT GRCh38
NC_000020.10:g.10393498_10393499delinsAT , CM000682.1:g.10393498_10393499delinsAT GRCh37
NC_000020.9:g.10341498_10341499delinsAT NCBI36
NG_009109.1:g.26368_26369delinsAT
NG_009109.2:g.26368_26369delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.664_665delinsAT ENSP00000498849.1:p.Met222=
ENST00000652676.1:n.459-151_459-150delinsAT
ENST00000347364.7:c.664_665delinsAT MANE Select ENSP00000246062.4:p.Met222=
ENST00000399054.6:c.664_665delinsAT ENSP00000382008.2:p.Met222=
NM_018848.3:c.664_665delinsAT NP_061336.1:p.Met222=
NM_170784.2:c.664_665delinsAT NP_740754.1:p.Met222=
NR_072977.1:n.364-4048_364-4047delinsAT
NR_072977.2:n.347-4048_347-4047delinsAT
NM_170784.3:c.664_665delinsAT MANE Select NP_740754.1:p.Met222=
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