Canonical Allele Identifier: CA509815433
Gene: MKKS HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.10393725A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10413077A>G , CM000682.2:g.10413077A>G GRCh38
NC_000020.10:g.10393725A>G , CM000682.1:g.10393725A>G GRCh37
NC_000020.9:g.10341725A>G NCBI36
NG_009109.1:g.26142T>C
NG_009109.2:g.26142T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000651692.1:c.438T>C ENSP00000498849.1:p.Ser146=
ENST00000652676.1:n.459-377T>C
ENST00000347364.7:c.438T>C MANE Select ENSP00000246062.4:p.Ser146=
ENST00000399054.6:c.438T>C ENSP00000382008.2:p.Ser146=
NM_018848.3:c.438T>C NP_061336.1:p.Ser146=
NM_170784.2:c.438T>C NP_740754.1:p.Ser146=
NR_072977.1:n.364-4274T>C
NR_072977.2:n.347-4274T>C
NM_170784.3:c.438T>C MANE Select NP_740754.1:p.Ser146=
Search 100 bp 5'
Search 100 bp 3'