Canonical Allele Identifier: CA1311924610

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558661G= , CM000664.2:g.181558661G=	GRCh38
NC_000002.11:g.182423388G= , CM000664.1:g.182423388G=	GRCh37
NC_000002.10:g.182131633G=	NCBI36
NG_021178.1:g.103447C=
NG_021178.2:g.103447C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-32C=	ENSP00000508396.1:n.-32C=
ENST00000410087.8:c.725C= MANE Select	ENSP00000386725.3:p.Ala242=
ENST00000339098.9:c.803C=	ENSP00000341159.5:p.Ala268=
ENST00000374967.6:c.661C=	ENSP00000364106.2:n.661C=
ENST00000374969.6:c.482-8953C=	ENSP00000364108.2:n.482-8953C=
ENST00000374970.6:c.614-8953C=	ENSP00000364109.2:n.614-8953C=
ENST00000409440.7:c.671C=	ENSP00000387080.3:p.Ala224=
ENST00000410087.7:c.725C=	ENSP00000386725.3:p.Ala242=
ENST00000421817.5:c.*7C=	ENSP00000411466.1:n.*7C=
ENST00000452174.5:c.529C=	ENSP00000409198.1:n.529C=
ENST00000466715.5:n.541C=
ENST00000479558.5:n.723C=
ENST00000494398.5:n.725C=
NM_001030311.2:c.803C=	NP_001025482.1:p.Ala268=
NM_001030312.2:c.482-8953C=	NP_001025483.1:n.482-8953C=
NM_001030313.2:c.614-8953C=	NP_001025484.1:n.614-8953C=
NM_001160277.1:c.671C=	NP_001153749.1:p.Ala224=
NM_201548.4:c.725C=	NP_963842.1:p.Ala242=
NR_027689.1:n.630C=
NR_027690.1:n.762C=
NM_201548.5:c.725C= MANE Select	NP_963842.1:p.Ala242=
NM_001030311.3:c.803C=	NP_001025482.1:p.Ala268=
NM_001030312.3:c.482-8953C=	NP_001025483.1:n.482-8953C=
NM_001030313.3:c.614-8953C=	NP_001025484.1:n.614-8953C=
NM_001160277.2:c.671C=	NP_001153749.1:p.Ala224=
NR_027689.2:n.628C=
NR_027690.2:n.760C=