Canonical Allele Identifier: CA2651912597
Gene: MKKS HGNC NCBI

Linked Data

ClinVar Variation Id: 2676543
ClinVar RCV Id: RCV003476474

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10413085del , CM000682.2:g.10413085del GRCh38
NC_000020.10:g.10393733del , CM000682.1:g.10393733del GRCh37
NC_000020.9:g.10341733del NCBI36
NG_009109.1:g.26136del
NG_009109.2:g.26136del

Transcript Alleles

HGVS Amino-acid change
ENST00000651692.1:c.432del ENSP00000498849.1:p.Phe144LeufsTer15
ENST00000652676.1:n.459-383del
ENST00000347364.7:c.432del MANE Select ENSP00000246062.4:p.Phe144LeufsTer15
ENST00000399054.6:c.432del ENSP00000382008.2:p.Phe144LeufsTer15
NM_018848.3:c.432del NP_061336.1:p.Phe144LeufsTer15
NM_170784.2:c.432del NP_740754.1:p.Phe144LeufsTer15
NR_072977.1:n.364-4280del
NR_072977.2:n.347-4280del
NM_170784.3:c.432del MANE Select NP_740754.1:p.Phe144LeufsTer15