Canonical Allele Identifier: CA2084402179

Gene: DCLK1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.35777609T= , CM000675.2:g.35777609T=	GRCh38
NC_000013.10:g.36351746T= , CM000675.1:g.36351746T=	GRCh37
NC_000013.9:g.35249746T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615680.5:c.1212-2910A=	ENSP00000484452.1:n.1212-2910A=
ENST00000360631.8:c.2059-2910A= MANE Select	ENSP00000353846.3:n.2059-2910A=
ENST00000255448.8:c.2133-2910A=	ENSP00000255448.4:n.2133-2910A=
ENST00000360631.7:c.2059-2910A=	ENSP00000353846.3:n.2059-2910A=
ENST00000379893.5:c.1138-2910A=	ENSP00000369223.1:n.1138-2910A=
ENST00000615680.4:c.1212-2910A=	ENSP00000484452.1:n.1212-2910A=
NM_001195415.1:c.1212-2910A=	NP_001182344.1:n.1212-2910A=
NM_001195416.1:c.1138-2910A=	NP_001182345.1:n.1138-2910A=
NM_004734.4:c.2133-2910A=	NP_004725.1:n.2133-2910A=
XM_005266592.2:c.2059-2910A=	XP_005266649.1:n.2059-2910A=
XM_006719893.2:c.2059-2910A=	XP_006719956.1:n.2059-2910A=
NM_001330071.1:c.2059-2910A=	NP_001317000.1:n.2059-2910A=
NM_001330072.1:c.2059-2910A=	NP_001317001.1:n.2059-2910A=
XM_017020847.1:c.2059-2899A=	XP_016876336.1:n.2059-2899A=
NM_001195416.2:c.1138-2910A=	NP_001182345.1:n.1138-2910A=
NM_001330071.2:c.2059-2910A= MANE Select	NP_001317000.1:n.2059-2910A=
NM_001330072.2:c.2059-2910A=	NP_001317001.1:n.2059-2910A=
NM_004734.5:c.2133-2910A=	NP_004725.1:n.2133-2910A=
NM_001195415.2:c.1212-2910A=	NP_001182344.1:n.1212-2910A=