Canonical Allele Identifier: CA1311924621

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558682G= , CM000664.2:g.181558682G=	GRCh38
NC_000002.11:g.182423409G= , CM000664.1:g.182423409G=	GRCh37
NC_000002.10:g.182131654G=	NCBI36
NG_021178.1:g.103426C=
NG_021178.2:g.103426C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-53C=	ENSP00000508396.1:n.-53C=
ENST00000410087.8:c.704C= MANE Select	ENSP00000386725.3:p.Ser235=
ENST00000339098.9:c.782C=	ENSP00000341159.5:p.Ser261=
ENST00000374967.6:c.640C=	ENSP00000364106.2:p.Leu214=
ENST00000374969.6:c.482-8974C=	ENSP00000364108.2:n.482-8974C=
ENST00000374970.6:c.614-8974C=	ENSP00000364109.2:n.614-8974C=
ENST00000409440.7:c.650C=	ENSP00000387080.3:p.Ser217=
ENST00000410087.7:c.704C=	ENSP00000386725.3:p.Ser235=
ENST00000421817.5:c.508C=	ENSP00000411466.1:p.Leu170=
ENST00000452174.5:c.508C=	ENSP00000409198.1:p.Leu170=
ENST00000466715.5:n.520C=
ENST00000479558.5:n.702C=
ENST00000494398.5:n.704C=
NM_001030311.2:c.782C=	NP_001025482.1:p.Ser261=
NM_001030312.2:c.482-8974C=	NP_001025483.1:n.482-8974C=
NM_001030313.2:c.614-8974C=	NP_001025484.1:n.614-8974C=
NM_001160277.1:c.650C=	NP_001153749.1:p.Ser217=
NM_201548.4:c.704C=	NP_963842.1:p.Ser235=
NR_027689.1:n.609C=
NR_027690.1:n.741C=
NM_201548.5:c.704C= MANE Select	NP_963842.1:p.Ser235=
NM_001030311.3:c.782C=	NP_001025482.1:p.Ser261=
NM_001030312.3:c.482-8974C=	NP_001025483.1:n.482-8974C=
NM_001030313.3:c.614-8974C=	NP_001025484.1:n.614-8974C=
NM_001160277.2:c.650C=	NP_001153749.1:p.Ser217=
NR_027689.2:n.607C=
NR_027690.2:n.739C=