Canonical Allele Identifier: CA1139666656
Gene: MKKS HGNC NCBI

Linked Data

ClinVar Variation Id: 992464
ClinVar RCV Id: RCV001280914

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412471_10413556del , CM000682.2:g.10412471_10413556del GRCh38
NC_000020.10:g.10393119_10394204del , CM000682.1:g.10393119_10394204del GRCh37
NC_000020.9:g.10341119_10342204del NCBI36
NG_009109.1:g.25664_26749del
NG_009109.2:g.25664_26749del

Transcript Alleles

HGVS Amino-acid change
ENST00000651692.1:c.-41_985+60del
ENST00000652676.1:n.458+241_629+60del
ENST00000347364.7:c.-41_985+60del
ENST00000399054.6:c.-41_985+60del
NM_018848.3:c.-41_985+60del
NM_170784.2:c.-41_985+60del
NR_072977.1:n.364-4752_364-3667del
NR_072977.2:n.347-4752_347-3667del
NM_170784.3:c.-41_985+60del