Canonical Allele Identifier: CA509814948
Gene: MKKS HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.10393275A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412627A>T , CM000682.2:g.10412627A>T GRCh38
NC_000020.10:g.10393275A>T , CM000682.1:g.10393275A>T GRCh37
NC_000020.9:g.10341275A>T NCBI36
NG_009109.1:g.26592T>A
NG_009109.2:g.26592T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.888T>A ENSP00000498849.1:p.Val296=
ENST00000652676.1:n.532T>A
ENST00000347364.7:c.888T>A MANE Select ENSP00000246062.4:p.Val296=
ENST00000399054.6:c.888T>A ENSP00000382008.2:p.Val296=
NM_018848.3:c.888T>A NP_061336.1:p.Val296=
NM_170784.2:c.888T>A NP_740754.1:p.Val296=
NR_072977.1:n.364-3824T>A
NR_072977.2:n.347-3824T>A
NM_170784.3:c.888T>A MANE Select NP_740754.1:p.Val296=