Canonical Allele Identifier: CA1961764972

Gene: DCDC1

Linked Data

• dbSNP Id: rs16921914

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.31189224G>T , CM000673.2:g.31189224G>T	GRCh38
NC_000011.9:g.31210771G>T , CM000673.1:g.31210771G>T	GRCh37
NC_000011.8:g.31167347G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000684477.1:c.1222-51440C>A MANE Select	ENSP00000507427.1:n.1222-51440C>A
ENST00000342355.8:c.*296+25946C>A	ENSP00000343496.4:n.*296+25946C>A
ENST00000534021.1:n.168-33161C>A
ENST00000534722.5:n.194-51440C>A
ENST00000597505.5:c.1222-51440C>A	ENSP00000472625.1:n.1222-51440C>A
NM_001350255.1:c.78+25946C>A	NP_001337184.1:n.78+25946C>A
XM_024448470.1:c.1222-51440C>A	XP_024304238.1:n.1222-51440C>A
XM_024448471.1:c.1222-51440C>A	XP_024304239.1:n.1222-51440C>A
XM_024448472.1:c.1222-51440C>A	XP_024304240.1:n.1222-51440C>A
XM_024448473.1:c.1222-51440C>A	XP_024304241.1:n.1222-51440C>A
XM_024448474.1:c.1222-51440C>A	XP_024304242.1:n.1222-51440C>A
XM_024448475.1:c.1222-51440C>A	XP_024304243.1:n.1222-51440C>A
XM_024448476.1:c.1222-51440C>A	XP_024304244.1:n.1222-51440C>A
XM_024448477.1:c.1222-51440C>A	XP_024304245.1:n.1222-51440C>A
XM_024448478.1:c.922-51440C>A	XP_024304246.1:n.922-51440C>A
XM_024448479.1:c.502-51440C>A	XP_024304247.1:n.502-51440C>A
XM_024448480.1:c.367-51440C>A	XP_024304248.1:n.367-51440C>A
XM_024448481.1:c.238-51440C>A	XP_024304249.1:n.238-51440C>A
XM_024448482.1:c.1222-51440C>A	XP_024304250.1:n.1222-51440C>A
XM_024448483.1:c.1222-51440C>A	XP_024304251.1:n.1222-51440C>A
XM_024448484.1:c.1222-51440C>A	XP_024304252.1:n.1222-51440C>A
XM_024448485.1:c.1222-51440C>A	XP_024304253.1:n.1222-51440C>A
XM_024448486.1:c.1222-51440C>A	XP_024304254.1:n.1222-51440C>A
XM_024448487.1:c.1222-51440C>A	XP_024304255.1:n.1222-51440C>A
XM_024448488.1:c.1222-51440C>A	XP_024304256.1:n.1222-51440C>A
XM_024448489.1:c.1222-51440C>A	XP_024304257.1:n.1222-51440C>A
XR_002957144.1:n.1460-51440C>A
XR_002957145.1:n.1460-51440C>A
NM_001367979.1:c.1222-51440C>A	NP_001354908.1:n.1222-51440C>A
NM_001387274.1:c.1222-51440C>A MANE Select	NP_001374203.1:n.1222-51440C>A
NR_170625.1:n.1276+25946C>A