Canonical Allele Identifier: CA1004469404
Gene: DIPK1A HGNC NCBI

Linked Data

dbSNP Id: rs992736030
gnomAD v3: 1-92936257-T-G
gnomAD v4: 1-92936257-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92936257T>G , CM000663.2:g.92936257T>G GRCh38
NC_000001.10:g.93401814T>G , CM000663.1:g.93401814T>G GRCh37
NC_000001.9:g.93174402T>G NCBI36
NG_033051.1:g.30266A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370310.5:c.54+25119A>C MANE Select ENSP00000359333.4:n.54+25119A>C
ENST00000370310.4:c.54+25119A>C ENSP00000359333.4:n.54+25119A>C
ENST00000613902.4:c.54+25119A>C ENSP00000484866.1:n.54+25119A>C
ENST00000615519.4:c.54+25119A>C ENSP00000483279.1:n.54+25119A>C
ENST00000616709.4:c.54+25119A>C ENSP00000482718.1:n.54+25119A>C
NM_001006605.4:c.54+25119A>C NP_001006606.2:n.54+25119A>C
NM_001252269.1:c.54+25119A>C NP_001239198.1:n.54+25119A>C
NM_001252270.1:c.54+25119A>C NP_001239199.1:n.54+25119A>C
NM_001252273.1:c.54+25119A>C NP_001239202.1:n.54+25119A>C
NM_001006605.5:c.54+25119A>C MANE Select NP_001006606.2:n.54+25119A>C
NM_001252269.2:c.54+25119A>C NP_001239198.1:n.54+25119A>C
NM_001252270.2:c.54+25119A>C NP_001239199.1:n.54+25119A>C
NM_001252273.2:c.54+25119A>C NP_001239202.1:n.54+25119A>C