Canonical Allele Identifier: CA798018685

Gene: DCK

Linked Data

• dbSNP Id: rs1214928527
• gnomAD v3: 4-71030456-T-C
• gnomAD v4: 4-71030456-T-C
• MyVariant Identifiers: chr4:g.71896173T>C (hg19) ; chr4:g.71030456T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71030456T>C , CM000666.2:g.71030456T>C	GRCh38
NC_000004.11:g.71896173T>C , CM000666.1:g.71896173T>C	GRCh37
NC_000004.10:g.72115037T>C	NCBI36
NG_023303.1:g.41909T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000286648.10:c.*1078T>C MANE Select	ENSP00000286648.5:n.*1078T>C
ENST00000286648.9:c.*1078T>C	ENSP00000286648.5:n.*1078T>C
ENST00000503359.5:c.*1805T>C	ENSP00000426389.1:n.*1805T>C
ENST00000504730.5:c.*1145T>C	ENSP00000425578.1:n.*1145T>C
ENST00000504952.1:c.*1004T>C	ENSP00000421508.1:n.*1004T>C
NM_000788.2:c.*1078T>C	NP_000779.1:n.*1078T>C
NM_000788.3:c.*1078T>C MANE Select	NP_000779.1:n.*1078T>C