Canonical Allele Identifier: CA510995052

Gene: DOK5

Linked Data

• MyVariant Identifiers: chr20:g.53267009T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54650470T>A , CM000682.2:g.54650470T>A	GRCh38
NC_000020.10:g.53267009T>A , CM000682.1:g.53267009T>A	GRCh37
NC_000020.9:g.52700416T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262593.10:c.912T>A MANE Select	ENSP00000262593.5:p.Ser304=
ENST00000262593.9:c.912T>A	ENSP00000262593.5:p.Ser304=
ENST00000395939.5:c.588T>A	ENSP00000379270.1:p.Ser196=
NM_018431.4:c.912T>A	NP_060901.2:p.Ser304=
NM_177959.2:c.588T>A	NP_808874.1:p.Ser196=
XM_011528903.1:c.876T>A	XP_011527205.1:p.Ser292=
XM_011528904.1:c.588T>A	XP_011527206.1:p.Ser196=
XM_024451946.1:c.876T>A	XP_024307714.1:p.Ser292=
NM_018431.5:c.912T>A MANE Select	NP_060901.2:p.Ser304=
NM_177959.3:c.588T>A	NP_808874.1:p.Ser196=