Canonical Allele Identifier: CA2349780950
Gene: MKKS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10413080_10413082delinsACT , CM000682.2:g.10413080_10413082delinsACT GRCh38
NC_000020.10:g.10393728_10393730delinsACT , CM000682.1:g.10393728_10393730delinsACT GRCh37
NC_000020.9:g.10341728_10341730delinsACT NCBI36
NG_009109.1:g.26137_26139delinsAGT
NG_009109.2:g.26137_26139delinsAGT

Transcript Alleles

HGVS Amino-acid change
ENST00000651692.1:c.433_435delinsAGT ENSP00000498849.1:p.Ser145=
ENST00000652676.1:n.459-382_459-380delinsAGT
ENST00000347364.7:c.433_435delinsAGT MANE Select ENSP00000246062.4:p.Ser145=
ENST00000399054.6:c.433_435delinsAGT ENSP00000382008.2:p.Ser145=
NM_018848.3:c.433_435delinsAGT NP_061336.1:p.Ser145=
NM_170784.2:c.433_435delinsAGT NP_740754.1:p.Ser145=
NR_072977.1:n.364-4279_364-4277delinsAGT
NR_072977.2:n.347-4279_347-4277delinsAGT
NM_170784.3:c.433_435delinsAGT MANE Select NP_740754.1:p.Ser145=