Canonical Allele Identifier: CA248117257

Gene: DCLK1

Linked Data

• dbSNP Id: rs939080535
• gnomAD v2: 13-36351653-G-C
• gnomAD v3: 13-35777516-G-C
• gnomAD v4: 13-35777516-G-C
• MyVariant Identifiers: chr13:g.36351653G>C (hg19) ; chr13:g.35777516G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.35777516G>C , CM000675.2:g.35777516G>C	GRCh38
NC_000013.10:g.36351653G>C , CM000675.1:g.36351653G>C	GRCh37
NC_000013.9:g.35249653G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000615680.5:c.1212-2817C>G	ENSP00000484452.1:n.1212-2817C>G
ENST00000360631.8:c.2059-2817C>G MANE Select	ENSP00000353846.3:n.2059-2817C>G
ENST00000255448.8:c.2133-2817C>G	ENSP00000255448.4:n.2133-2817C>G
ENST00000360631.7:c.2059-2817C>G	ENSP00000353846.3:n.2059-2817C>G
ENST00000379893.5:c.1138-2817C>G	ENSP00000369223.1:n.1138-2817C>G
ENST00000615680.4:c.1212-2817C>G	ENSP00000484452.1:n.1212-2817C>G
NM_001195415.1:c.1212-2817C>G	NP_001182344.1:n.1212-2817C>G
NM_001195416.1:c.1138-2817C>G	NP_001182345.1:n.1138-2817C>G
NM_004734.4:c.2133-2817C>G	NP_004725.1:n.2133-2817C>G
XM_005266592.2:c.2059-2817C>G	XP_005266649.1:n.2059-2817C>G
XM_006719893.2:c.2059-2817C>G	XP_006719956.1:n.2059-2817C>G
NM_001330071.1:c.2059-2817C>G	NP_001317000.1:n.2059-2817C>G
NM_001330072.1:c.2059-2817C>G	NP_001317001.1:n.2059-2817C>G
XM_017020847.1:c.2059-2806C>G	XP_016876336.1:n.2059-2806C>G
NM_001195416.2:c.1138-2817C>G	NP_001182345.1:n.1138-2817C>G
NM_001330071.2:c.2059-2817C>G MANE Select	NP_001317000.1:n.2059-2817C>G
NM_001330072.2:c.2059-2817C>G	NP_001317001.1:n.2059-2817C>G
NM_004734.5:c.2133-2817C>G	NP_004725.1:n.2133-2817C>G
NM_001195415.2:c.1212-2817C>G	NP_001182344.1:n.1212-2817C>G