Canonical Allele Identifier: CA2670931568
Gene: DCK HGNC NCBI

Linked Data

gnomAD v4: 4-71030457-G-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030457G>T , CM000666.2:g.71030457G>T GRCh38
NC_000004.11:g.71896174G>T , CM000666.1:g.71896174G>T GRCh37
NC_000004.10:g.72115038G>T NCBI36
NG_023303.1:g.41910G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1079G>T MANE Select ENSP00000286648.5:n.*1079G>T
ENST00000286648.9:c.*1079G>T ENSP00000286648.5:n.*1079G>T
ENST00000503359.5:c.*1806G>T ENSP00000426389.1:n.*1806G>T
ENST00000504730.5:c.*1146G>T ENSP00000425578.1:n.*1146G>T
ENST00000504952.1:c.*1005G>T ENSP00000421508.1:n.*1005G>T
NM_000788.2:c.*1079G>T NP_000779.1:n.*1079G>T
NM_000788.3:c.*1079G>T MANE Select NP_000779.1:n.*1079G>T
Search 100 bp 5'
Search 100 bp 3'