Canonical Allele Identifier: CA348298122

Gene: CKAP2L

Linked Data

• dbSNP Id: rs1680558091
• gnomAD v3: 2-112756883-A-G
• gnomAD v4: 2-112756883-A-G
• MyVariant Identifiers: chr2:g.113514460A>G (hg19) ; chr2:g.112756883A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756883A>G , CM000664.2:g.112756883A>G	GRCh38
NC_000002.11:g.113514460A>G , CM000664.1:g.113514460A>G	GRCh37
NC_000002.10:g.113230931A>G	NCBI36
NG_041820.1:g.12795T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.488T>C MANE Select	ENSP00000305204.6:p.Ile163Thr
ENST00000302450.10:c.488T>C	ENSP00000305204.6:p.Ile163Thr
ENST00000435431.5:c.478+10T>C	ENSP00000414834.1:n.478+10T>C
ENST00000481732.5:n.449T>C
NM_001304361.1:c.-8T>C	NP_001291290.1:n.-8T>C
NM_152515.4:c.488T>C	NP_689728.3:p.Ile163Thr
NR_130712.1:n.557+10T>C
XM_011510666.1:c.-8T>C	XP_011508968.1:n.-8T>C
XM_011510666.2:c.-8T>C	XP_011508968.1:n.-8T>C
NM_152515.5:c.488T>C MANE Select	NP_689728.3:p.Ile163Thr
NM_001304361.2:c.-8T>C	NP_001291290.1:n.-8T>C
NR_130712.2:n.489+10T>C