Canonical Allele Identifier: CA348297726

Gene: CKAP2L

Linked Data

• MyVariant Identifiers: chr2:g.113514288A>T (hg19) ; chr2:g.112756711A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.112756711A>T , CM000664.2:g.112756711A>T	GRCh38
NC_000002.11:g.113514288A>T , CM000664.1:g.113514288A>T	GRCh37
NC_000002.10:g.113230759A>T	NCBI36
NG_041820.1:g.12967T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302450.11:c.660T>A MANE Select	ENSP00000305204.6:p.Ser220Arg
ENST00000302450.10:c.660T>A	ENSP00000305204.6:p.Ser220Arg
ENST00000435431.5:c.478+182T>A	ENSP00000414834.1:n.478+182T>A
NM_001304361.1:c.165T>A	NP_001291290.1:p.Ser55Arg
NM_152515.4:c.660T>A	NP_689728.3:p.Ser220Arg
NR_130712.1:n.557+182T>A
XM_011510666.1:c.165T>A	XP_011508968.1:p.Ser55Arg
XM_011510666.2:c.165T>A	XP_011508968.1:p.Ser55Arg
NM_152515.5:c.660T>A MANE Select	NP_689728.3:p.Ser220Arg
NM_001304361.2:c.165T>A	NP_001291290.1:p.Ser55Arg
NR_130712.2:n.489+182T>A