Canonical Allele Identifier: CA1961709651

Gene: DCDC1

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.31057572G>C , CM000673.2:g.31057572G>C	GRCh38
NC_000011.9:g.31079119G>C , CM000673.1:g.31079119G>C	GRCh37
NC_000011.8:g.31035695G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684477.1:c.2591+6897C>G MANE Select	ENSP00000507427.1:n.2591+6897C>G
ENST00000342355.8:c.*1666+6897C>G	ENSP00000343496.4:n.*1666+6897C>G
ENST00000437348.5:n.1299+6897C>G
ENST00000597505.5:c.2591+6897C>G	ENSP00000472625.1:n.2591+6897C>G
NM_001350255.1:c.1448+6897C>G	NP_001337184.1:n.1448+6897C>G
XM_024448470.1:c.2591+6897C>G	XP_024304238.1:n.2591+6897C>G
XM_024448471.1:c.2591+6897C>G	XP_024304239.1:n.2591+6897C>G
XM_024448472.1:c.2591+6897C>G	XP_024304240.1:n.2591+6897C>G
XM_024448473.1:c.2591+6897C>G	XP_024304241.1:n.2591+6897C>G
XM_024448474.1:c.2591+6897C>G	XP_024304242.1:n.2591+6897C>G
XM_024448475.1:c.2591+6897C>G	XP_024304243.1:n.2591+6897C>G
XM_024448476.1:c.2456+6897C>G	XP_024304244.1:n.2456+6897C>G
XM_024448477.1:c.2591+6897C>G	XP_024304245.1:n.2591+6897C>G
XM_024448478.1:c.2291+6897C>G	XP_024304246.1:n.2291+6897C>G
XM_024448479.1:c.1871+6897C>G	XP_024304247.1:n.1871+6897C>G
XM_024448480.1:c.1736+6897C>G	XP_024304248.1:n.1736+6897C>G
XM_024448481.1:c.1607+6897C>G	XP_024304249.1:n.1607+6897C>G
XM_024448482.1:c.2591+6897C>G	XP_024304250.1:n.2591+6897C>G
XM_024448483.1:c.2591+6897C>G	XP_024304251.1:n.2591+6897C>G
XM_024448484.1:c.2591+6897C>G	XP_024304252.1:n.2591+6897C>G
XM_024448485.1:c.2591+6897C>G	XP_024304253.1:n.2591+6897C>G
XR_002957144.1:n.2829+6897C>G
NM_001367979.1:c.2591+6897C>G	NP_001354908.1:n.2591+6897C>G
NM_001387274.1:c.2591+6897C>G MANE Select	NP_001374203.1:n.2591+6897C>G
NR_170625.1:n.2646+6897C>G