Canonical Allele Identifier: CA2084402212
Gene: DCLK1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.35777693T= , CM000675.2:g.35777693T= GRCh38
NC_000013.10:g.36351830T= , CM000675.1:g.36351830T= GRCh37
NC_000013.9:g.35249830T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000615680.5:c.1212-2994A= ENSP00000484452.1:n.1212-2994A=
ENST00000360631.8:c.2059-2994A= MANE Select ENSP00000353846.3:n.2059-2994A=
ENST00000255448.8:c.2133-2994A= ENSP00000255448.4:n.2133-2994A=
ENST00000360631.7:c.2059-2994A= ENSP00000353846.3:n.2059-2994A=
ENST00000379893.5:c.1138-2994A= ENSP00000369223.1:n.1138-2994A=
ENST00000615680.4:c.1212-2994A= ENSP00000484452.1:n.1212-2994A=
NM_001195415.1:c.1212-2994A= NP_001182344.1:n.1212-2994A=
NM_001195416.1:c.1138-2994A= NP_001182345.1:n.1138-2994A=
NM_004734.4:c.2133-2994A= NP_004725.1:n.2133-2994A=
XM_005266592.2:c.2059-2994A= XP_005266649.1:n.2059-2994A=
XM_006719893.2:c.2059-2994A= XP_006719956.1:n.2059-2994A=
NM_001330071.1:c.2059-2994A= NP_001317000.1:n.2059-2994A=
NM_001330072.1:c.2059-2994A= NP_001317001.1:n.2059-2994A=
XM_017020847.1:c.2059-2983A= XP_016876336.1:n.2059-2983A=
NM_001195416.2:c.1138-2994A= NP_001182345.1:n.1138-2994A=
NM_001330071.2:c.2059-2994A= MANE Select NP_001317000.1:n.2059-2994A=
NM_001330072.2:c.2059-2994A= NP_001317001.1:n.2059-2994A=
NM_004734.5:c.2133-2994A= NP_004725.1:n.2133-2994A=
NM_001195415.2:c.1212-2994A= NP_001182344.1:n.1212-2994A=