Canonical Allele Identifier: CA428553833

Gene: CKAP2L

Linked Data

• MyVariant Identifiers: chr2:g.113514240A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756663A>G , CM000664.2:g.112756663A>G	GRCh38
NC_000002.11:g.113514240A>G , CM000664.1:g.113514240A>G	GRCh37
NC_000002.10:g.113230711A>G	NCBI36
NG_041820.1:g.13015T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.708T>C MANE Select	ENSP00000305204.6:p.Val236=
ENST00000302450.10:c.708T>C	ENSP00000305204.6:p.Val236=
ENST00000435431.5:c.478+230T>C	ENSP00000414834.1:n.478+230T>C
NM_001304361.1:c.213T>C	NP_001291290.1:p.Val71=
NM_152515.4:c.708T>C	NP_689728.3:p.Val236=
NR_130712.1:n.557+230T>C
XM_011510666.1:c.213T>C	XP_011508968.1:p.Val71=
XM_011510666.2:c.213T>C	XP_011508968.1:p.Val71=
NM_152515.5:c.708T>C MANE Select	NP_689728.3:p.Val236=
NM_001304361.2:c.213T>C	NP_001291290.1:p.Val71=
NR_130712.2:n.489+230T>C