Canonical Allele Identifier: CA1311924609

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558654A= , CM000664.2:g.181558654A=	GRCh38
NC_000002.11:g.182423381A= , CM000664.1:g.182423381A=	GRCh37
NC_000002.10:g.182131626A=	NCBI36
NG_021178.1:g.103454T=
NG_021178.2:g.103454T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-25T=	ENSP00000508396.1:n.-25T=
ENST00000410087.8:c.732T= MANE Select	ENSP00000386725.3:p.Leu244=
ENST00000339098.9:c.810T=	ENSP00000341159.5:p.Leu270=
ENST00000374967.6:c.668T=	ENSP00000364106.2:n.668T=
ENST00000374969.6:c.482-8946T=	ENSP00000364108.2:n.482-8946T=
ENST00000374970.6:c.614-8946T=	ENSP00000364109.2:n.614-8946T=
ENST00000409440.7:c.678T=	ENSP00000387080.3:p.Leu226=
ENST00000410087.7:c.732T=	ENSP00000386725.3:p.Leu244=
ENST00000421817.5:c.*14T=	ENSP00000411466.1:n.*14T=
ENST00000452174.5:c.536T=	ENSP00000409198.1:n.536T=
ENST00000466715.5:n.548T=
ENST00000479558.5:n.730T=
ENST00000494398.5:n.732T=
NM_001030311.2:c.810T=	NP_001025482.1:p.Leu270=
NM_001030312.2:c.482-8946T=	NP_001025483.1:n.482-8946T=
NM_001030313.2:c.614-8946T=	NP_001025484.1:n.614-8946T=
NM_001160277.1:c.678T=	NP_001153749.1:p.Leu226=
NM_201548.4:c.732T=	NP_963842.1:p.Leu244=
NR_027689.1:n.637T=
NR_027690.1:n.769T=
NM_201548.5:c.732T= MANE Select	NP_963842.1:p.Leu244=
NM_001030311.3:c.810T=	NP_001025482.1:p.Leu270=
NM_001030312.3:c.482-8946T=	NP_001025483.1:n.482-8946T=
NM_001030313.3:c.614-8946T=	NP_001025484.1:n.614-8946T=
NM_001160277.2:c.678T=	NP_001153749.1:p.Leu226=
NR_027689.2:n.635T=
NR_027690.2:n.767T=