Canonical Allele Identifier: CA509815169

Gene: MKKS

Linked Data

• MyVariant Identifiers: chr20:g.10393566A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.10412918A>G , CM000682.2:g.10412918A>G	GRCh38
NC_000020.10:g.10393566A>G , CM000682.1:g.10393566A>G	GRCh37
NC_000020.9:g.10341566A>G	NCBI36
NG_009109.1:g.26301T>C
NG_009109.2:g.26301T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651692.1:c.597T>C	ENSP00000498849.1:p.Ser199=
ENST00000652676.1:n.459-218T>C
ENST00000347364.7:c.597T>C MANE Select	ENSP00000246062.4:p.Ser199=
ENST00000399054.6:c.597T>C	ENSP00000382008.2:p.Ser199=
NM_018848.3:c.597T>C	NP_061336.1:p.Ser199=
NM_170784.2:c.597T>C	NP_740754.1:p.Ser199=
NR_072977.1:n.364-4115T>C
NR_072977.2:n.347-4115T>C
NM_170784.3:c.597T>C MANE Select	NP_740754.1:p.Ser199=