Canonical Allele Identifier: CA248117394

Gene: DCLK1

Linked Data

• dbSNP Id: rs776090823
• gnomAD v3: 13-35777651-A-G
• gnomAD v4: 13-35777651-A-G
• MyVariant Identifiers: chr13:g.36351788A>G (hg19) ; chr13:g.35777651A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.35777651A>G , CM000675.2:g.35777651A>G	GRCh38
NC_000013.10:g.36351788A>G , CM000675.1:g.36351788A>G	GRCh37
NC_000013.9:g.35249788A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000615680.5:c.1212-2952T>C	ENSP00000484452.1:n.1212-2952T>C
ENST00000360631.8:c.2059-2952T>C MANE Select	ENSP00000353846.3:n.2059-2952T>C
ENST00000255448.8:c.2133-2952T>C	ENSP00000255448.4:n.2133-2952T>C
ENST00000360631.7:c.2059-2952T>C	ENSP00000353846.3:n.2059-2952T>C
ENST00000379893.5:c.1138-2952T>C	ENSP00000369223.1:n.1138-2952T>C
ENST00000615680.4:c.1212-2952T>C	ENSP00000484452.1:n.1212-2952T>C
NM_001195415.1:c.1212-2952T>C	NP_001182344.1:n.1212-2952T>C
NM_001195416.1:c.1138-2952T>C	NP_001182345.1:n.1138-2952T>C
NM_004734.4:c.2133-2952T>C	NP_004725.1:n.2133-2952T>C
XM_005266592.2:c.2059-2952T>C	XP_005266649.1:n.2059-2952T>C
XM_006719893.2:c.2059-2952T>C	XP_006719956.1:n.2059-2952T>C
NM_001330071.1:c.2059-2952T>C	NP_001317000.1:n.2059-2952T>C
NM_001330072.1:c.2059-2952T>C	NP_001317001.1:n.2059-2952T>C
XM_017020847.1:c.2059-2941T>C	XP_016876336.1:n.2059-2941T>C
NM_001195416.2:c.1138-2952T>C	NP_001182345.1:n.1138-2952T>C
NM_001330071.2:c.2059-2952T>C MANE Select	NP_001317000.1:n.2059-2952T>C
NM_001330072.2:c.2059-2952T>C	NP_001317001.1:n.2059-2952T>C
NM_004734.5:c.2133-2952T>C	NP_004725.1:n.2133-2952T>C
NM_001195415.2:c.1212-2952T>C	NP_001182344.1:n.1212-2952T>C