Canonical Allele Identifier: CA348297555

Gene: CKAP2L

Linked Data

• dbSNP Id: rs758072975
• gnomAD v3: 2-112756635-C-A
• gnomAD v4: 2-112756635-C-A
• MyVariant Identifiers: chr2:g.113514212C>A (hg19) ; chr2:g.112756635C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756635C>A , CM000664.2:g.112756635C>A	GRCh38
NC_000002.11:g.113514212C>A , CM000664.1:g.113514212C>A	GRCh37
NC_000002.10:g.113230683C>A	NCBI36
NG_041820.1:g.13043G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.736G>T MANE Select	ENSP00000305204.6:p.Val246Phe
ENST00000302450.10:c.736G>T	ENSP00000305204.6:p.Val246Phe
ENST00000435431.5:c.478+258G>T	ENSP00000414834.1:n.478+258G>T
NM_001304361.1:c.241G>T	NP_001291290.1:p.Val81Phe
NM_152515.4:c.736G>T	NP_689728.3:p.Val246Phe
NR_130712.1:n.557+258G>T
XM_011510666.1:c.241G>T	XP_011508968.1:p.Val81Phe
XM_011510666.2:c.241G>T	XP_011508968.1:p.Val81Phe
NM_152515.5:c.736G>T MANE Select	NP_689728.3:p.Val246Phe
NM_001304361.2:c.241G>T	NP_001291290.1:p.Val81Phe
NR_130712.2:n.489+258G>T