Canonical Allele Identifier: CA1467008439

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70996957T>G , CM000666.2:g.70996957T>G GRCh38
NC_000004.11:g.71862674T>G , CM000666.1:g.71862674T>G GRCh37
NC_000004.10:g.72081538T>G NCBI36
NG_023303.1:g.8410T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.92-1110T>G (DCK) MANE Select ENSP00000286648.5:n.92-1110T>G
ENST00000286648.9:c.92-1110T>G (DCK) ENSP00000286648.5:n.92-1110T>G
ENST00000503359.5:c.*36-1110T>G (DCK) ENSP00000426389.1:n.*36-1110T>G
ENST00000504730.5:c.92-1110T>G (DCK) ENSP00000425578.1:n.92-1110T>G
ENST00000504952.1:c.92-1110T>G (DCK) ENSP00000421508.1:n.92-1110T>G
ENST00000511449.1:n.429-1110T>G (MOB1B)
NM_000788.2:c.92-1110T>G (DCK) NP_000779.1:n.92-1110T>G
NM_000788.3:c.92-1110T>G (DCK) MANE Select NP_000779.1:n.92-1110T>G