Canonical Allele Identifier: CA2670931567

Gene: DCK

Linked Data

• gnomAD v4: 4-71030451-G-GT

Genomic Alleles

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

Transcript Alleles

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