Canonical Allele Identifier: CA349740203

Gene: CERKL

Linked Data

• MyVariant Identifiers: chr2:g.182423324T>G (hg19) ; chr2:g.181558597T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558597T>G , CM000664.2:g.181558597T>G	GRCh38
NC_000002.11:g.182423324T>G , CM000664.1:g.182423324T>G	GRCh37
NC_000002.10:g.182131569T>G	NCBI36
NG_021178.1:g.103511A>C
NG_021178.2:g.103511A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.33A>C	ENSP00000508396.1:p.Arg11Ser
ENST00000410087.8:c.789A>C MANE Select	ENSP00000386725.3:p.Arg263Ser
ENST00000339098.9:c.867A>C	ENSP00000341159.5:p.Arg289Ser
ENST00000374967.6:c.725A>C	ENSP00000364106.2:n.725A>C
ENST00000374969.6:c.482-8889A>C	ENSP00000364108.2:n.482-8889A>C
ENST00000374970.6:c.614-8889A>C	ENSP00000364109.2:n.614-8889A>C
ENST00000409440.7:c.735A>C	ENSP00000387080.3:p.Arg245Ser
ENST00000410087.7:c.789A>C	ENSP00000386725.3:p.Arg263Ser
ENST00000421817.5:c.*71A>C	ENSP00000411466.1:n.*71A>C
ENST00000452174.5:c.593A>C	ENSP00000409198.1:n.593A>C
ENST00000479558.5:n.787A>C
ENST00000494398.5:n.789A>C
NM_001030311.2:c.867A>C	NP_001025482.1:p.Arg289Ser
NM_001030312.2:c.482-8889A>C	NP_001025483.1:n.482-8889A>C
NM_001030313.2:c.614-8889A>C	NP_001025484.1:n.614-8889A>C
NM_001160277.1:c.735A>C	NP_001153749.1:p.Arg245Ser
NM_201548.4:c.789A>C	NP_963842.1:p.Arg263Ser
NR_027689.1:n.694A>C
NR_027690.1:n.826A>C
NM_201548.5:c.789A>C MANE Select	NP_963842.1:p.Arg263Ser
NM_001030311.3:c.867A>C	NP_001025482.1:p.Arg289Ser
NM_001030312.3:c.482-8889A>C	NP_001025483.1:n.482-8889A>C
NM_001030313.3:c.614-8889A>C	NP_001025484.1:n.614-8889A>C
NM_001160277.2:c.735A>C	NP_001153749.1:p.Arg245Ser
NR_027689.2:n.692A>C
NR_027690.2:n.824A>C