Canonical Allele Identifier: CA430407699

Gene: CERKL

Linked Data

• MyVariant Identifiers: chr2:g.182423357C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558630C>T , CM000664.2:g.181558630C>T	GRCh38
NC_000002.11:g.182423357C>T , CM000664.1:g.182423357C>T	GRCh37
NC_000002.10:g.182131602C>T	NCBI36
NG_021178.1:g.103478G>A
NG_021178.2:g.103478G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-1G>A	ENSP00000508396.1:n.-1G>A
ENST00000410087.8:c.756G>A MANE Select	ENSP00000386725.3:p.Gly252=
ENST00000339098.9:c.834G>A	ENSP00000341159.5:p.Gly278=
ENST00000374967.6:c.692G>A	ENSP00000364106.2:n.692G>A
ENST00000374969.6:c.482-8922G>A	ENSP00000364108.2:n.482-8922G>A
ENST00000374970.6:c.614-8922G>A	ENSP00000364109.2:n.614-8922G>A
ENST00000409440.7:c.702G>A	ENSP00000387080.3:p.Gly234=
ENST00000410087.7:c.756G>A	ENSP00000386725.3:p.Gly252=
ENST00000421817.5:c.*38G>A	ENSP00000411466.1:n.*38G>A
ENST00000452174.5:c.560G>A	ENSP00000409198.1:n.560G>A
ENST00000479558.5:n.754G>A
ENST00000494398.5:n.756G>A
NM_001030311.2:c.834G>A	NP_001025482.1:p.Gly278=
NM_001030312.2:c.482-8922G>A	NP_001025483.1:n.482-8922G>A
NM_001030313.2:c.614-8922G>A	NP_001025484.1:n.614-8922G>A
NM_001160277.1:c.702G>A	NP_001153749.1:p.Gly234=
NM_201548.4:c.756G>A	NP_963842.1:p.Gly252=
NR_027689.1:n.661G>A
NR_027690.1:n.793G>A
NM_201548.5:c.756G>A MANE Select	NP_963842.1:p.Gly252=
NM_001030311.3:c.834G>A	NP_001025482.1:p.Gly278=
NM_001030312.3:c.482-8922G>A	NP_001025483.1:n.482-8922G>A
NM_001030313.3:c.614-8922G>A	NP_001025484.1:n.614-8922G>A
NM_001160277.2:c.702G>A	NP_001153749.1:p.Gly234=
NR_027689.2:n.659G>A
NR_027690.2:n.791G>A