Canonical Allele Identifier: CA1311924623

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558687A= , CM000664.2:g.181558687A=	GRCh38
NC_000002.11:g.182423414A= , CM000664.1:g.182423414A=	GRCh37
NC_000002.10:g.182131659A=	NCBI36
NG_021178.1:g.103421T=
NG_021178.2:g.103421T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-58T=	ENSP00000508396.1:n.-58T=
ENST00000410087.8:c.699T= MANE Select	ENSP00000386725.3:p.Asp233=
ENST00000339098.9:c.777T=	ENSP00000341159.5:p.Asp259=
ENST00000374967.6:c.635T=	ENSP00000364106.2:p.Met212=
ENST00000374969.6:c.482-8979T=	ENSP00000364108.2:n.482-8979T=
ENST00000374970.6:c.614-8979T=	ENSP00000364109.2:n.614-8979T=
ENST00000409440.7:c.645T=	ENSP00000387080.3:p.Asp215=
ENST00000410087.7:c.699T=	ENSP00000386725.3:p.Asp233=
ENST00000421817.5:c.503T=	ENSP00000411466.1:p.Met168=
ENST00000452174.5:c.503T=	ENSP00000409198.1:p.Met168=
ENST00000466715.5:n.515T=
ENST00000479558.5:n.697T=
ENST00000494398.5:n.699T=
NM_001030311.2:c.777T=	NP_001025482.1:p.Asp259=
NM_001030312.2:c.482-8979T=	NP_001025483.1:n.482-8979T=
NM_001030313.2:c.614-8979T=	NP_001025484.1:n.614-8979T=
NM_001160277.1:c.645T=	NP_001153749.1:p.Asp215=
NM_201548.4:c.699T=	NP_963842.1:p.Asp233=
NR_027689.1:n.604T=
NR_027690.1:n.736T=
NM_201548.5:c.699T= MANE Select	NP_963842.1:p.Asp233=
NM_001030311.3:c.777T=	NP_001025482.1:p.Asp259=
NM_001030312.3:c.482-8979T=	NP_001025483.1:n.482-8979T=
NM_001030313.3:c.614-8979T=	NP_001025484.1:n.614-8979T=
NM_001160277.2:c.645T=	NP_001153749.1:p.Asp215=
NR_027689.2:n.602T=
NR_027690.2:n.734T=