Canonical Allele Identifier: CA349741147

Gene: CERKL

Linked Data

• dbSNP Id: rs1688312028
• gnomAD v3: 2-181558706-A-G
• gnomAD v4: 2-181558706-A-G
• MyVariant Identifiers: chr2:g.182423433A>G (hg19) ; chr2:g.181558706A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558706A>G , CM000664.2:g.181558706A>G	GRCh38
NC_000002.11:g.182423433A>G , CM000664.1:g.182423433A>G	GRCh37
NC_000002.10:g.182131678A>G	NCBI36
NG_021178.1:g.103402T>C
NG_021178.2:g.103402T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-77T>C	ENSP00000508396.1:n.-77T>C
ENST00000410087.8:c.680T>C MANE Select	ENSP00000386725.3:p.Val227Ala
ENST00000339098.9:c.758T>C	ENSP00000341159.5:p.Val253Ala
ENST00000374967.6:c.616T>C	ENSP00000364106.2:p.Leu206=
ENST00000374969.6:c.482-8998T>C	ENSP00000364108.2:n.482-8998T>C
ENST00000374970.6:c.614-8998T>C	ENSP00000364109.2:n.614-8998T>C
ENST00000409440.7:c.626T>C	ENSP00000387080.3:p.Val209Ala
ENST00000410087.7:c.680T>C	ENSP00000386725.3:p.Val227Ala
ENST00000421817.5:c.484T>C	ENSP00000411466.1:p.Leu162=
ENST00000452174.5:c.484T>C	ENSP00000409198.1:p.Leu162=
ENST00000466715.5:n.496T>C
ENST00000479558.5:n.678T>C
ENST00000494398.5:n.680T>C
NM_001030311.2:c.758T>C	NP_001025482.1:p.Val253Ala
NM_001030312.2:c.482-8998T>C	NP_001025483.1:n.482-8998T>C
NM_001030313.2:c.614-8998T>C	NP_001025484.1:n.614-8998T>C
NM_001160277.1:c.626T>C	NP_001153749.1:p.Val209Ala
NM_201548.4:c.680T>C	NP_963842.1:p.Val227Ala
NR_027689.1:n.585T>C
NR_027690.1:n.717T>C
NM_201548.5:c.680T>C MANE Select	NP_963842.1:p.Val227Ala
NM_001030311.3:c.758T>C	NP_001025482.1:p.Val253Ala
NM_001030312.3:c.482-8998T>C	NP_001025483.1:n.482-8998T>C
NM_001030313.3:c.614-8998T>C	NP_001025484.1:n.614-8998T>C
NM_001160277.2:c.626T>C	NP_001153749.1:p.Val209Ala
NR_027689.2:n.583T>C
NR_027690.2:n.715T>C