Canonical Allele Identifier: CA798018683

Gene: DCK

Linked Data

• dbSNP Id: rs1240319009
• gnomAD v3: 4-71030442-G-T
• gnomAD v4: 4-71030442-G-T
• MyVariant Identifiers: chr4:g.71896159G>T (hg19) ; chr4:g.71030442G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71030442G>T , CM000666.2:g.71030442G>T	GRCh38
NC_000004.11:g.71896159G>T , CM000666.1:g.71896159G>T	GRCh37
NC_000004.10:g.72115023G>T	NCBI36
NG_023303.1:g.41895G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286648.10:c.*1064G>T MANE Select	ENSP00000286648.5:n.*1064G>T
ENST00000286648.9:c.*1064G>T	ENSP00000286648.5:n.*1064G>T
ENST00000503359.5:c.*1791G>T	ENSP00000426389.1:n.*1791G>T
ENST00000504730.5:c.*1131G>T	ENSP00000425578.1:n.*1131G>T
ENST00000504952.1:c.*990G>T	ENSP00000421508.1:n.*990G>T
NM_000788.2:c.*1064G>T	NP_000779.1:n.*1064G>T
NM_000788.3:c.*1064G>T MANE Select	NP_000779.1:n.*1064G>T