Canonical Allele Identifier: CA1311924486

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558342A= , CM000664.2:g.181558342A=	GRCh38
NC_000002.11:g.182423069A= , CM000664.1:g.182423069A=	GRCh37
NC_000002.10:g.182131314A=	NCBI36
NG_021178.1:g.103766T=
NG_021178.2:g.103766T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.64+224T=	ENSP00000508396.1:n.64+224T=
ENST00000410087.8:c.820+224T= MANE Select	ENSP00000386725.3:n.820+224T=
ENST00000339098.9:c.898+224T=	ENSP00000341159.5:n.898+224T=
ENST00000374967.6:c.756+224T=	ENSP00000364106.2:n.756+224T=
ENST00000374969.6:c.482-8634T=	ENSP00000364108.2:n.482-8634T=
ENST00000374970.6:c.614-8634T=	ENSP00000364109.2:n.614-8634T=
ENST00000409440.7:c.766+224T=	ENSP00000387080.3:n.766+224T=
ENST00000410087.7:c.820+224T=	ENSP00000386725.3:n.820+224T=
ENST00000421817.5:c.*102+224T=	ENSP00000411466.1:n.*102+224T=
ENST00000452174.5:c.624+224T=	ENSP00000409198.1:n.624+224T=
ENST00000479558.5:n.818+224T=
ENST00000494398.5:n.820+224T=
NM_001030311.2:c.898+224T=	NP_001025482.1:n.898+224T=
NM_001030312.2:c.482-8634T=	NP_001025483.1:n.482-8634T=
NM_001030313.2:c.614-8634T=	NP_001025484.1:n.614-8634T=
NM_001160277.1:c.766+224T=	NP_001153749.1:n.766+224T=
NM_201548.4:c.820+224T=	NP_963842.1:n.820+224T=
NR_027689.1:n.725+224T=
NR_027690.1:n.857+224T=
NM_201548.5:c.820+224T= MANE Select	NP_963842.1:n.820+224T=
NM_001030311.3:c.898+224T=	NP_001025482.1:n.898+224T=
NM_001030312.3:c.482-8634T=	NP_001025483.1:n.482-8634T=
NM_001030313.3:c.614-8634T=	NP_001025484.1:n.614-8634T=
NM_001160277.2:c.766+224T=	NP_001153749.1:n.766+224T=
NR_027689.2:n.723+224T=
NR_027690.2:n.855+224T=