Canonical Allele Identifier: CA348297887

Gene: CKAP2L

Linked Data

• MyVariant Identifiers: chr2:g.113514357C>G (hg19) ; chr2:g.112756780C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756780C>G , CM000664.2:g.112756780C>G	GRCh38
NC_000002.11:g.113514357C>G , CM000664.1:g.113514357C>G	GRCh37
NC_000002.10:g.113230828C>G	NCBI36
NG_041820.1:g.12898G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.591G>C MANE Select	ENSP00000305204.6:p.Arg197Ser
ENST00000302450.10:c.591G>C	ENSP00000305204.6:p.Arg197Ser
ENST00000435431.5:c.478+113G>C	ENSP00000414834.1:n.478+113G>C
ENST00000481732.5:n.552G>C
NM_001304361.1:c.96G>C	NP_001291290.1:p.Arg32Ser
NM_152515.4:c.591G>C	NP_689728.3:p.Arg197Ser
NR_130712.1:n.557+113G>C
XM_011510666.1:c.96G>C	XP_011508968.1:p.Arg32Ser
XM_011510666.2:c.96G>C	XP_011508968.1:p.Arg32Ser
NM_152515.5:c.591G>C MANE Select	NP_689728.3:p.Arg197Ser
NM_001304361.2:c.96G>C	NP_001291290.1:p.Arg32Ser
NR_130712.2:n.489+113G>C