Canonical Allele Identifier: CA348298099

Gene: CKAP2L

Linked Data

• MyVariant Identifiers: chr2:g.113514451A>C (hg19) ; chr2:g.112756874A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756874A>C , CM000664.2:g.112756874A>C	GRCh38
NC_000002.11:g.113514451A>C , CM000664.1:g.113514451A>C	GRCh37
NC_000002.10:g.113230922A>C	NCBI36
NG_041820.1:g.12804T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.497T>G MANE Select	ENSP00000305204.6:p.Met166Arg
ENST00000302450.10:c.497T>G	ENSP00000305204.6:p.Met166Arg
ENST00000435431.5:c.478+19T>G	ENSP00000414834.1:n.478+19T>G
ENST00000481732.5:n.458T>G
NM_001304361.1:c.2T>G	NP_001291290.1:p.Met1Arg
NM_152515.4:c.497T>G	NP_689728.3:p.Met166Arg
NR_130712.1:n.557+19T>G
XM_011510666.1:c.2T>G	XP_011508968.1:p.Met1Arg
XM_011510666.2:c.2T>G	XP_011508968.1:p.Met1Arg
NM_152515.5:c.497T>G MANE Select	NP_689728.3:p.Met166Arg
NM_001304361.2:c.2T>G	NP_001291290.1:p.Met1Arg
NR_130712.2:n.489+19T>G