Canonical Allele Identifier: CA348297948

Gene: CKAP2L

Linked Data

• MyVariant Identifiers: chr2:g.113514386A>T (hg19) ; chr2:g.112756809A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756809A>T , CM000664.2:g.112756809A>T	GRCh38
NC_000002.11:g.113514386A>T , CM000664.1:g.113514386A>T	GRCh37
NC_000002.10:g.113230857A>T	NCBI36
NG_041820.1:g.12869T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.562T>A MANE Select	ENSP00000305204.6:p.Leu188Met
ENST00000302450.10:c.562T>A	ENSP00000305204.6:p.Leu188Met
ENST00000435431.5:c.478+84T>A	ENSP00000414834.1:n.478+84T>A
ENST00000481732.5:n.523T>A
NM_001304361.1:c.67T>A	NP_001291290.1:p.Leu23Met
NM_152515.4:c.562T>A	NP_689728.3:p.Leu188Met
NR_130712.1:n.557+84T>A
XM_011510666.1:c.67T>A	XP_011508968.1:p.Leu23Met
XM_011510666.2:c.67T>A	XP_011508968.1:p.Leu23Met
NM_152515.5:c.562T>A MANE Select	NP_689728.3:p.Leu188Met
NM_001304361.2:c.67T>A	NP_001291290.1:p.Leu23Met
NR_130712.2:n.489+84T>A