Canonical Allele Identifier: CA349740859

Gene: CERKL

Linked Data

• MyVariant Identifiers: chr2:g.182423390A>T (hg19) ; chr2:g.181558663A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558663A>T , CM000664.2:g.181558663A>T	GRCh38
NC_000002.11:g.182423390A>T , CM000664.1:g.182423390A>T	GRCh37
NC_000002.10:g.182131635A>T	NCBI36
NG_021178.1:g.103445T>A
NG_021178.2:g.103445T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-34T>A	ENSP00000508396.1:n.-34T>A
ENST00000410087.8:c.723T>A MANE Select	ENSP00000386725.3:p.His241Gln
ENST00000339098.9:c.801T>A	ENSP00000341159.5:p.His267Gln
ENST00000374967.6:c.659T>A	ENSP00000364106.2:n.659T>A
ENST00000374969.6:c.482-8955T>A	ENSP00000364108.2:n.482-8955T>A
ENST00000374970.6:c.614-8955T>A	ENSP00000364109.2:n.614-8955T>A
ENST00000409440.7:c.669T>A	ENSP00000387080.3:p.His223Gln
ENST00000410087.7:c.723T>A	ENSP00000386725.3:p.His241Gln
ENST00000421817.5:c.*5T>A	ENSP00000411466.1:n.*5T>A
ENST00000452174.5:c.527T>A	ENSP00000409198.1:n.527T>A
ENST00000466715.5:n.539T>A
ENST00000479558.5:n.721T>A
ENST00000494398.5:n.723T>A
NM_001030311.2:c.801T>A	NP_001025482.1:p.His267Gln
NM_001030312.2:c.482-8955T>A	NP_001025483.1:n.482-8955T>A
NM_001030313.2:c.614-8955T>A	NP_001025484.1:n.614-8955T>A
NM_001160277.1:c.669T>A	NP_001153749.1:p.His223Gln
NM_201548.4:c.723T>A	NP_963842.1:p.His241Gln
NR_027689.1:n.628T>A
NR_027690.1:n.760T>A
NM_201548.5:c.723T>A MANE Select	NP_963842.1:p.His241Gln
NM_001030311.3:c.801T>A	NP_001025482.1:p.His267Gln
NM_001030312.3:c.482-8955T>A	NP_001025483.1:n.482-8955T>A
NM_001030313.3:c.614-8955T>A	NP_001025484.1:n.614-8955T>A
NM_001160277.2:c.669T>A	NP_001153749.1:p.His223Gln
NR_027689.2:n.626T>A
NR_027690.2:n.758T>A