Canonical Allele Identifier: CA428554296

Gene: CKAP2L

Linked Data

• MyVariant Identifiers: chr2:g.113514381G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756804G>C , CM000664.2:g.112756804G>C	GRCh38
NC_000002.11:g.113514381G>C , CM000664.1:g.113514381G>C	GRCh37
NC_000002.10:g.113230852G>C	NCBI36
NG_041820.1:g.12874C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.567C>G MANE Select	ENSP00000305204.6:p.Leu189=
ENST00000302450.10:c.567C>G	ENSP00000305204.6:p.Leu189=
ENST00000435431.5:c.478+89C>G	ENSP00000414834.1:n.478+89C>G
ENST00000481732.5:n.528C>G
NM_001304361.1:c.72C>G	NP_001291290.1:p.Leu24=
NM_152515.4:c.567C>G	NP_689728.3:p.Leu189=
NR_130712.1:n.557+89C>G
XM_011510666.1:c.72C>G	XP_011508968.1:p.Leu24=
XM_011510666.2:c.72C>G	XP_011508968.1:p.Leu24=
NM_152515.5:c.567C>G MANE Select	NP_689728.3:p.Leu189=
NM_001304361.2:c.72C>G	NP_001291290.1:p.Leu24=
NR_130712.2:n.489+89C>G