Canonical Allele Identifier: CA1311924619

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558679G= , CM000664.2:g.181558679G=	GRCh38
NC_000002.11:g.182423406G= , CM000664.1:g.182423406G=	GRCh37
NC_000002.10:g.182131651G=	NCBI36
NG_021178.1:g.103429C=
NG_021178.2:g.103429C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-50C=	ENSP00000508396.1:n.-50C=
ENST00000410087.8:c.707C= MANE Select	ENSP00000386725.3:p.Ala236=
ENST00000339098.9:c.785C=	ENSP00000341159.5:p.Ala262=
ENST00000374967.6:c.643C=	ENSP00000364106.2:p.Leu215=
ENST00000374969.6:c.482-8971C=	ENSP00000364108.2:n.482-8971C=
ENST00000374970.6:c.614-8971C=	ENSP00000364109.2:n.614-8971C=
ENST00000409440.7:c.653C=	ENSP00000387080.3:p.Ala218=
ENST00000410087.7:c.707C=	ENSP00000386725.3:p.Ala236=
ENST00000421817.5:c.511C=	ENSP00000411466.1:p.Leu171=
ENST00000452174.5:c.511C=	ENSP00000409198.1:p.Leu171=
ENST00000466715.5:n.523C=
ENST00000479558.5:n.705C=
ENST00000494398.5:n.707C=
NM_001030311.2:c.785C=	NP_001025482.1:p.Ala262=
NM_001030312.2:c.482-8971C=	NP_001025483.1:n.482-8971C=
NM_001030313.2:c.614-8971C=	NP_001025484.1:n.614-8971C=
NM_001160277.1:c.653C=	NP_001153749.1:p.Ala218=
NM_201548.4:c.707C=	NP_963842.1:p.Ala236=
NR_027689.1:n.612C=
NR_027690.1:n.744C=
NM_201548.5:c.707C= MANE Select	NP_963842.1:p.Ala236=
NM_001030311.3:c.785C=	NP_001025482.1:p.Ala262=
NM_001030312.3:c.482-8971C=	NP_001025483.1:n.482-8971C=
NM_001030313.3:c.614-8971C=	NP_001025484.1:n.614-8971C=
NM_001160277.2:c.653C=	NP_001153749.1:p.Ala218=
NR_027689.2:n.610C=
NR_027690.2:n.742C=