Canonical Allele Identifier: CA2084427141
Gene: DCLK1 HGNC NCBI

Linked Data

dbSNP Id: rs1872794584

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.35880000C>G , CM000675.2:g.35880000C>G GRCh38
NC_000013.10:g.36454137C>G , CM000675.1:g.36454137C>G GRCh37
NC_000013.9:g.35352137C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360631.8:c.824-8660G>C MANE Select ENSP00000353846.3:n.824-8660G>C
ENST00000255448.8:c.824-8660G>C ENSP00000255448.4:n.824-8660G>C
ENST00000360631.7:c.824-8660G>C ENSP00000353846.3:n.824-8660G>C
ENST00000379892.4:c.824-8660G>C ENSP00000369222.4:n.824-8660G>C
NM_004734.4:c.824-8660G>C NP_004725.1:n.824-8660G>C
XM_005266592.2:c.824-8660G>C XP_005266649.1:n.824-8660G>C
XM_006719893.2:c.824-8660G>C XP_006719956.1:n.824-8660G>C
XR_941855.1:n.1312-16627C>G
NM_001330071.1:c.824-8660G>C NP_001317000.1:n.824-8660G>C
NM_001330072.1:c.824-8660G>C NP_001317001.1:n.824-8660G>C
XM_017020847.1:c.824-8660G>C XP_016876336.1:n.824-8660G>C
XM_017020848.1:c.824-8660G>C XP_016876337.1:n.824-8660G>C
XR_001749821.1:n.77-16627C>G
XR_941855.2:n.77-16627C>G
NM_001330071.2:c.824-8660G>C MANE Select NP_001317000.1:n.824-8660G>C
NM_001330072.2:c.824-8660G>C NP_001317001.1:n.824-8660G>C
NM_004734.5:c.824-8660G>C NP_004725.1:n.824-8660G>C