Canonical Allele Identifier: CA408232668
Gene: MKKS HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.10393525G>T (hg19) chr20:g.10412877G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10412877G>T , CM000682.2:g.10412877G>T GRCh38
NC_000020.10:g.10393525G>T , CM000682.1:g.10393525G>T GRCh37
NC_000020.9:g.10341525G>T NCBI36
NG_009109.1:g.26342C>A
NG_009109.2:g.26342C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000651692.1:c.638C>A ENSP00000498849.1:p.Thr213Asn
ENST00000652676.1:n.459-177C>A
ENST00000347364.7:c.638C>A MANE Select ENSP00000246062.4:p.Thr213Asn
ENST00000399054.6:c.638C>A ENSP00000382008.2:p.Thr213Asn
NM_018848.3:c.638C>A NP_061336.1:p.Thr213Asn
NM_170784.2:c.638C>A NP_740754.1:p.Thr213Asn
NR_072977.1:n.364-4074C>A
NR_072977.2:n.347-4074C>A
NM_170784.3:c.638C>A MANE Select NP_740754.1:p.Thr213Asn
Search 100 bp 5'
Search 100 bp 3'