Canonical Allele Identifier: CA428554193

Gene: CKAP2L

Linked Data

• dbSNP Id: rs1385627192
• gnomAD v3: 2-112756606-T-C
• gnomAD v4: 2-112756606-T-C
• MyVariant Identifiers: chr2:g.113514183T>C (hg19) ; chr2:g.112756606T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756606T>C , CM000664.2:g.112756606T>C	GRCh38
NC_000002.11:g.113514183T>C , CM000664.1:g.113514183T>C	GRCh37
NC_000002.10:g.113230654T>C	NCBI36
NG_041820.1:g.13072A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.765A>G MANE Select	ENSP00000305204.6:p.Pro255=
ENST00000302450.10:c.765A>G	ENSP00000305204.6:p.Pro255=
ENST00000435431.5:c.478+287A>G	ENSP00000414834.1:n.478+287A>G
NM_001304361.1:c.270A>G	NP_001291290.1:p.Pro90=
NM_152515.4:c.765A>G	NP_689728.3:p.Pro255=
NR_130712.1:n.557+287A>G
XM_011510666.1:c.270A>G	XP_011508968.1:p.Pro90=
XM_011510666.2:c.270A>G	XP_011508968.1:p.Pro90=
NM_152515.5:c.765A>G MANE Select	NP_689728.3:p.Pro255=
NM_001304361.2:c.270A>G	NP_001291290.1:p.Pro90=
NR_130712.2:n.489+287A>G