Canonical Allele Identifier: CA342696062

Gene: CLK2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.155268012C>A , CM000663.2:g.155268012C>A	GRCh38
NC_000001.10:g.155237803C>A , CM000663.1:g.155237803C>A	GRCh37
NC_000001.9:g.153504427C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001294338.2:c.669G>T MANE Select	NP_001281267.1:p.Lys223Asn
ENST00000368361.9:c.669G>T MANE Select	ENSP00000357345.4:p.Lys223Asn
NM_001294338.1:c.669G>T	NP_001281267.1:p.Lys223Asn
NM_001294339.1:c.-16G>T	NP_001281268.1:n.-16G>T
NM_001294339.2:c.-16G>T	NP_001281268.1:n.-16G>T
NM_001363704.1:c.663G>T	NP_001350633.1:p.Lys221Asn
NM_001363704.2:c.663G>T	NP_001350633.1:p.Lys221Asn
NM_003993.3:c.666G>T	NP_003984.2:p.Lys222Asn
NM_003993.4:c.666G>T	NP_003984.2:p.Lys222Asn
ENST00000355560.4:c.663G>T	ENSP00000347759.4:p.Lys221Asn
ENST00000361168.9:c.666G>T	ENSP00000354856.5:p.Lys222Asn
ENST00000368361.8:c.669G>T	ENSP00000357345.4:p.Lys223Asn
ENST00000476983.5:n.710G>T
ENST00000497188.1:n.1186G>T
XM_005244878.1:c.663G>T	XP_005244935.1:p.Lys221Asn
XM_011509143.1:c.666G>T	XP_011507445.1:p.Lys222Asn
XM_011509143.2:c.666G>T	XP_011507445.1:p.Lys222Asn
XM_011509144.1:c.669G>T	XP_011507446.1:p.Lys223Asn
XM_011509145.1:c.23G>T	XP_011507447.1:p.Arg8Ile
XM_011509146.1:c.23G>T	XP_011507448.1:p.Arg8Ile
XM_011509147.1:c.23G>T	XP_011507449.1:p.Arg8Ile
XR_241067.2:n.983G>T