Canonical Allele Identifier: CA348297926

Gene: CKAP2L

Linked Data

• COSMIC: COSM3836619
• MyVariant Identifiers: chr2:g.113514376A>T (hg19) ; chr2:g.112756799A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756799A>T , CM000664.2:g.112756799A>T	GRCh38
NC_000002.11:g.113514376A>T , CM000664.1:g.113514376A>T	GRCh37
NC_000002.10:g.113230847A>T	NCBI36
NG_041820.1:g.12879T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.572T>A MANE Select	ENSP00000305204.6:p.Ile191Asn
ENST00000302450.10:c.572T>A	ENSP00000305204.6:p.Ile191Asn
ENST00000435431.5:c.478+94T>A	ENSP00000414834.1:n.478+94T>A
ENST00000481732.5:n.533T>A
NM_001304361.1:c.77T>A	NP_001291290.1:p.Ile26Asn
NM_152515.4:c.572T>A	NP_689728.3:p.Ile191Asn
NR_130712.1:n.557+94T>A
XM_011510666.1:c.77T>A	XP_011508968.1:p.Ile26Asn
XM_011510666.2:c.77T>A	XP_011508968.1:p.Ile26Asn
NM_152515.5:c.572T>A MANE Select	NP_689728.3:p.Ile191Asn
NM_001304361.2:c.77T>A	NP_001291290.1:p.Ile26Asn
NR_130712.2:n.489+94T>A