Canonical Allele Identifier: CA1311924577

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558579G= , CM000664.2:g.181558579G=	GRCh38
NC_000002.11:g.182423306G= , CM000664.1:g.182423306G=	GRCh37
NC_000002.10:g.182131551G=	NCBI36
NG_021178.1:g.103529C=
NG_021178.2:g.103529C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.51C=	ENSP00000508396.1:p.Gly17=
ENST00000410087.8:c.807C= MANE Select	ENSP00000386725.3:p.Gly269=
ENST00000339098.9:c.885C=	ENSP00000341159.5:p.Gly295=
ENST00000374967.6:c.743C=	ENSP00000364106.2:n.743C=
ENST00000374969.6:c.482-8871C=	ENSP00000364108.2:n.482-8871C=
ENST00000374970.6:c.614-8871C=	ENSP00000364109.2:n.614-8871C=
ENST00000409440.7:c.753C=	ENSP00000387080.3:p.Gly251=
ENST00000410087.7:c.807C=	ENSP00000386725.3:p.Gly269=
ENST00000421817.5:c.*89C=	ENSP00000411466.1:n.*89C=
ENST00000452174.5:c.611C=	ENSP00000409198.1:n.611C=
ENST00000479558.5:n.805C=
ENST00000494398.5:n.807C=
NM_001030311.2:c.885C=	NP_001025482.1:p.Gly295=
NM_001030312.2:c.482-8871C=	NP_001025483.1:n.482-8871C=
NM_001030313.2:c.614-8871C=	NP_001025484.1:n.614-8871C=
NM_001160277.1:c.753C=	NP_001153749.1:p.Gly251=
NM_201548.4:c.807C=	NP_963842.1:p.Gly269=
NR_027689.1:n.712C=
NR_027690.1:n.844C=
NM_201548.5:c.807C= MANE Select	NP_963842.1:p.Gly269=
NM_001030311.3:c.885C=	NP_001025482.1:p.Gly295=
NM_001030312.3:c.482-8871C=	NP_001025483.1:n.482-8871C=
NM_001030313.3:c.614-8871C=	NP_001025484.1:n.614-8871C=
NM_001160277.2:c.753C=	NP_001153749.1:p.Gly251=
NR_027689.2:n.710C=
NR_027690.2:n.842C=