Canonical Allele Identifier: CA1311924598

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558623T= , CM000664.2:g.181558623T=	GRCh38
NC_000002.11:g.182423350T= , CM000664.1:g.182423350T=	GRCh37
NC_000002.10:g.182131595T=	NCBI36
NG_021178.1:g.103485A=
NG_021178.2:g.103485A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.7A=	ENSP00000508396.1:p.Thr3=
ENST00000410087.8:c.763A= MANE Select	ENSP00000386725.3:p.Thr255=
ENST00000339098.9:c.841A=	ENSP00000341159.5:p.Thr281=
ENST00000374967.6:c.699A=	ENSP00000364106.2:n.699A=
ENST00000374969.6:c.482-8915A=	ENSP00000364108.2:n.482-8915A=
ENST00000374970.6:c.614-8915A=	ENSP00000364109.2:n.614-8915A=
ENST00000409440.7:c.709A=	ENSP00000387080.3:p.Thr237=
ENST00000410087.7:c.763A=	ENSP00000386725.3:p.Thr255=
ENST00000421817.5:c.*45A=	ENSP00000411466.1:n.*45A=
ENST00000452174.5:c.567A=	ENSP00000409198.1:n.567A=
ENST00000479558.5:n.761A=
ENST00000494398.5:n.763A=
NM_001030311.2:c.841A=	NP_001025482.1:p.Thr281=
NM_001030312.2:c.482-8915A=	NP_001025483.1:n.482-8915A=
NM_001030313.2:c.614-8915A=	NP_001025484.1:n.614-8915A=
NM_001160277.1:c.709A=	NP_001153749.1:p.Thr237=
NM_201548.4:c.763A=	NP_963842.1:p.Thr255=
NR_027689.1:n.668A=
NR_027690.1:n.800A=
NM_201548.5:c.763A= MANE Select	NP_963842.1:p.Thr255=
NM_001030311.3:c.841A=	NP_001025482.1:p.Thr281=
NM_001030312.3:c.482-8915A=	NP_001025483.1:n.482-8915A=
NM_001030313.3:c.614-8915A=	NP_001025484.1:n.614-8915A=
NM_001160277.2:c.709A=	NP_001153749.1:p.Thr237=
NR_027689.2:n.666A=
NR_027690.2:n.798A=