Canonical Allele Identifier: CA2084427145

Gene: DCLK1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.35880016A= , CM000675.2:g.35880016A=	GRCh38
NC_000013.10:g.36454153A= , CM000675.1:g.36454153A=	GRCh37
NC_000013.9:g.35352153A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360631.8:c.824-8676T= MANE Select	ENSP00000353846.3:n.824-8676T=
ENST00000255448.8:c.824-8676T=	ENSP00000255448.4:n.824-8676T=
ENST00000360631.7:c.824-8676T=	ENSP00000353846.3:n.824-8676T=
ENST00000379892.4:c.824-8676T=	ENSP00000369222.4:n.824-8676T=
NM_004734.4:c.824-8676T=	NP_004725.1:n.824-8676T=
XM_005266592.2:c.824-8676T=	XP_005266649.1:n.824-8676T=
XM_006719893.2:c.824-8676T=	XP_006719956.1:n.824-8676T=
XR_941855.1:n.1312-16611A=
NM_001330071.1:c.824-8676T=	NP_001317000.1:n.824-8676T=
NM_001330072.1:c.824-8676T=	NP_001317001.1:n.824-8676T=
XM_017020847.1:c.824-8676T=	XP_016876336.1:n.824-8676T=
XM_017020848.1:c.824-8676T=	XP_016876337.1:n.824-8676T=
XR_001749821.1:n.77-16611A=
XR_941855.2:n.77-16611A=
NM_001330071.2:c.824-8676T= MANE Select	NP_001317000.1:n.824-8676T=
NM_001330072.2:c.824-8676T=	NP_001317001.1:n.824-8676T=
NM_004734.5:c.824-8676T=	NP_004725.1:n.824-8676T=