Canonical Allele Identifier: CA1311924585

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558593G= , CM000664.2:g.181558593G=	GRCh38
NC_000002.11:g.182423320G= , CM000664.1:g.182423320G=	GRCh37
NC_000002.10:g.182131565G=	NCBI36
NG_021178.1:g.103515C=
NG_021178.2:g.103515C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.37C=	ENSP00000508396.1:p.Gln13=
ENST00000410087.8:c.793C= MANE Select	ENSP00000386725.3:p.Gln265=
ENST00000339098.9:c.871C=	ENSP00000341159.5:p.Gln291=
ENST00000374967.6:c.729C=	ENSP00000364106.2:n.729C=
ENST00000374969.6:c.482-8885C=	ENSP00000364108.2:n.482-8885C=
ENST00000374970.6:c.614-8885C=	ENSP00000364109.2:n.614-8885C=
ENST00000409440.7:c.739C=	ENSP00000387080.3:p.Gln247=
ENST00000410087.7:c.793C=	ENSP00000386725.3:p.Gln265=
ENST00000421817.5:c.*75C=	ENSP00000411466.1:n.*75C=
ENST00000452174.5:c.597C=	ENSP00000409198.1:n.597C=
ENST00000479558.5:n.791C=
ENST00000494398.5:n.793C=
NM_001030311.2:c.871C=	NP_001025482.1:p.Gln291=
NM_001030312.2:c.482-8885C=	NP_001025483.1:n.482-8885C=
NM_001030313.2:c.614-8885C=	NP_001025484.1:n.614-8885C=
NM_001160277.1:c.739C=	NP_001153749.1:p.Gln247=
NM_201548.4:c.793C=	NP_963842.1:p.Gln265=
NR_027689.1:n.698C=
NR_027690.1:n.830C=
NM_201548.5:c.793C= MANE Select	NP_963842.1:p.Gln265=
NM_001030311.3:c.871C=	NP_001025482.1:p.Gln291=
NM_001030312.3:c.482-8885C=	NP_001025483.1:n.482-8885C=
NM_001030313.3:c.614-8885C=	NP_001025484.1:n.614-8885C=
NM_001160277.2:c.739C=	NP_001153749.1:p.Gln247=
NR_027689.2:n.696C=
NR_027690.2:n.828C=