Canonical Allele Identifier: CA428554039

Gene: CKAP2L

Linked Data

• MyVariant Identifiers: chr2:g.113514084T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756507T>C , CM000664.2:g.112756507T>C	GRCh38
NC_000002.11:g.113514084T>C , CM000664.1:g.113514084T>C	GRCh37
NC_000002.10:g.113230555T>C	NCBI36
NG_041820.1:g.13171A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.864A>G MANE Select	ENSP00000305204.6:p.Lys288=
ENST00000302450.10:c.864A>G	ENSP00000305204.6:p.Lys288=
ENST00000435431.5:c.479-373A>G	ENSP00000414834.1:n.479-373A>G
NM_001304361.1:c.369A>G	NP_001291290.1:p.Lys123=
NM_152515.4:c.864A>G	NP_689728.3:p.Lys288=
NR_130712.1:n.558-373A>G
XM_011510666.1:c.369A>G	XP_011508968.1:p.Lys123=
XM_011510666.2:c.369A>G	XP_011508968.1:p.Lys123=
NM_152515.5:c.864A>G MANE Select	NP_689728.3:p.Lys288=
NM_001304361.2:c.369A>G	NP_001291290.1:p.Lys123=
NR_130712.2:n.490-373A>G