Canonical Allele Identifier: CA348297727

Gene: CKAP2L

Linked Data

• gnomAD v4: 2-112756712-C-A
• MyVariant Identifiers: chr2:g.113514289C>A (hg19) ; chr2:g.112756712C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756712C>A , CM000664.2:g.112756712C>A	GRCh38
NC_000002.11:g.113514289C>A , CM000664.1:g.113514289C>A	GRCh37
NC_000002.10:g.113230760C>A	NCBI36
NG_041820.1:g.12966G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.659G>T MANE Select	ENSP00000305204.6:p.Ser220Ile
ENST00000302450.10:c.659G>T	ENSP00000305204.6:p.Ser220Ile
ENST00000435431.5:c.478+181G>T	ENSP00000414834.1:n.478+181G>T
NM_001304361.1:c.164G>T	NP_001291290.1:p.Ser55Ile
NM_152515.4:c.659G>T	NP_689728.3:p.Ser220Ile
NR_130712.1:n.557+181G>T
XM_011510666.1:c.164G>T	XP_011508968.1:p.Ser55Ile
XM_011510666.2:c.164G>T	XP_011508968.1:p.Ser55Ile
NM_152515.5:c.659G>T MANE Select	NP_689728.3:p.Ser220Ile
NM_001304361.2:c.164G>T	NP_001291290.1:p.Ser55Ile
NR_130712.2:n.489+181G>T