Canonical Allele Identifier: CA348297604

Gene: CKAP2L

Linked Data

• dbSNP Id: rs1386814073
• gnomAD v2: 2-113514232-T-C
• gnomAD v4: 2-112756655-T-C
• MyVariant Identifiers: chr2:g.113514232T>C (hg19) ; chr2:g.112756655T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756655T>C , CM000664.2:g.112756655T>C	GRCh38
NC_000002.11:g.113514232T>C , CM000664.1:g.113514232T>C	GRCh37
NC_000002.10:g.113230703T>C	NCBI36
NG_041820.1:g.13023A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.716A>G MANE Select	ENSP00000305204.6:p.Asp239Gly
ENST00000302450.10:c.716A>G	ENSP00000305204.6:p.Asp239Gly
ENST00000435431.5:c.478+238A>G	ENSP00000414834.1:n.478+238A>G
NM_001304361.1:c.221A>G	NP_001291290.1:p.Asp74Gly
NM_152515.4:c.716A>G	NP_689728.3:p.Asp239Gly
NR_130712.1:n.557+238A>G
XM_011510666.1:c.221A>G	XP_011508968.1:p.Asp74Gly
XM_011510666.2:c.221A>G	XP_011508968.1:p.Asp74Gly
NM_152515.5:c.716A>G MANE Select	NP_689728.3:p.Asp239Gly
NM_001304361.2:c.221A>G	NP_001291290.1:p.Asp74Gly
NR_130712.2:n.489+238A>G