Canonical Allele Identifier: CA408232172

Gene: MKKS

Linked Data

• gnomAD v4: 20-10412641-G-T
• MyVariant Identifiers: chr20:g.10393289G>T (hg19) ; chr20:g.10412641G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.10412641G>T , CM000682.2:g.10412641G>T	GRCh38
NC_000020.10:g.10393289G>T , CM000682.1:g.10393289G>T	GRCh37
NC_000020.9:g.10341289G>T	NCBI36
NG_009109.1:g.26578C>A
NG_009109.2:g.26578C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651692.1:c.874C>A	ENSP00000498849.1:p.Leu292Met
ENST00000652676.1:n.518C>A
ENST00000347364.7:c.874C>A MANE Select	ENSP00000246062.4:p.Leu292Met
ENST00000399054.6:c.874C>A	ENSP00000382008.2:p.Leu292Met
NM_018848.3:c.874C>A	NP_061336.1:p.Leu292Met
NM_170784.2:c.874C>A	NP_740754.1:p.Leu292Met
NR_072977.1:n.364-3838C>A
NR_072977.2:n.347-3838C>A
NM_170784.3:c.874C>A MANE Select	NP_740754.1:p.Leu292Met