Canonical Allele Identifier: CA349740214

Gene: CERKL

Linked Data

• MyVariant Identifiers: chr2:g.182423328A>G (hg19) ; chr2:g.181558601A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558601A>G , CM000664.2:g.181558601A>G	GRCh38
NC_000002.11:g.182423328A>G , CM000664.1:g.182423328A>G	GRCh37
NC_000002.10:g.182131573A>G	NCBI36
NG_021178.1:g.103507T>C
NG_021178.2:g.103507T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.29T>C	ENSP00000508396.1:p.Val10Ala
ENST00000410087.8:c.785T>C MANE Select	ENSP00000386725.3:p.Val262Ala
ENST00000339098.9:c.863T>C	ENSP00000341159.5:p.Val288Ala
ENST00000374967.6:c.721T>C	ENSP00000364106.2:n.721T>C
ENST00000374969.6:c.482-8893T>C	ENSP00000364108.2:n.482-8893T>C
ENST00000374970.6:c.614-8893T>C	ENSP00000364109.2:n.614-8893T>C
ENST00000409440.7:c.731T>C	ENSP00000387080.3:p.Val244Ala
ENST00000410087.7:c.785T>C	ENSP00000386725.3:p.Val262Ala
ENST00000421817.5:c.*67T>C	ENSP00000411466.1:n.*67T>C
ENST00000452174.5:c.589T>C	ENSP00000409198.1:n.589T>C
ENST00000479558.5:n.783T>C
ENST00000494398.5:n.785T>C
NM_001030311.2:c.863T>C	NP_001025482.1:p.Val288Ala
NM_001030312.2:c.482-8893T>C	NP_001025483.1:n.482-8893T>C
NM_001030313.2:c.614-8893T>C	NP_001025484.1:n.614-8893T>C
NM_001160277.1:c.731T>C	NP_001153749.1:p.Val244Ala
NM_201548.4:c.785T>C	NP_963842.1:p.Val262Ala
NR_027689.1:n.690T>C
NR_027690.1:n.822T>C
NM_201548.5:c.785T>C MANE Select	NP_963842.1:p.Val262Ala
NM_001030311.3:c.863T>C	NP_001025482.1:p.Val288Ala
NM_001030312.3:c.482-8893T>C	NP_001025483.1:n.482-8893T>C
NM_001030313.3:c.614-8893T>C	NP_001025484.1:n.614-8893T>C
NM_001160277.2:c.731T>C	NP_001153749.1:p.Val244Ala
NR_027689.2:n.688T>C
NR_027690.2:n.820T>C