Canonical Allele Identifier: CA348297958

Gene: CKAP2L

Linked Data

• MyVariant Identifiers: chr2:g.113514391T>A (hg19) ; chr2:g.112756814T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756814T>A , CM000664.2:g.112756814T>A	GRCh38
NC_000002.11:g.113514391T>A , CM000664.1:g.113514391T>A	GRCh37
NC_000002.10:g.113230862T>A	NCBI36
NG_041820.1:g.12864A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.557A>T MANE Select	ENSP00000305204.6:p.Glu186Val
ENST00000302450.10:c.557A>T	ENSP00000305204.6:p.Glu186Val
ENST00000435431.5:c.478+79A>T	ENSP00000414834.1:n.478+79A>T
ENST00000481732.5:n.518A>T
NM_001304361.1:c.62A>T	NP_001291290.1:p.Glu21Val
NM_152515.4:c.557A>T	NP_689728.3:p.Glu186Val
NR_130712.1:n.557+79A>T
XM_011510666.1:c.62A>T	XP_011508968.1:p.Glu21Val
XM_011510666.2:c.62A>T	XP_011508968.1:p.Glu21Val
NM_152515.5:c.557A>T MANE Select	NP_689728.3:p.Glu186Val
NM_001304361.2:c.62A>T	NP_001291290.1:p.Glu21Val
NR_130712.2:n.489+79A>T