Canonical Allele Identifier: CA233690

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181573777C>A , CM000664.2:g.181573777C>A	GRCh38
NC_000002.11:g.182438504C>A , CM000664.1:g.182438504C>A	GRCh37
NC_000002.10:g.182146749C>A	NCBI36
NG_021178.1:g.88331G>T
NG_021178.2:g.88331G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-104G>T	ENSP00000508396.1:n.-104G>T
ENST00000410087.8:c.589G>T MANE Select	ENSP00000386725.3:p.Ala197Ser
ENST00000339098.9:c.589G>T	ENSP00000341159.5:p.Ala197Ser
ENST00000374967.6:c.589G>T	ENSP00000364106.2:p.Ala197Ser
ENST00000374969.6:c.482-24069G>T	ENSP00000364108.2:n.482-24069G>T
ENST00000374970.6:c.589G>T	ENSP00000364109.2:p.Ala197Ser
ENST00000409440.7:c.482-7656G>T	ENSP00000387080.3:n.482-7656G>T
ENST00000410087.7:c.589G>T	ENSP00000386725.3:p.Ala197Ser
ENST00000421817.5:c.482-15069G>T	ENSP00000411466.1:n.482-15069G>T
ENST00000452174.5:c.482-15069G>T	ENSP00000409198.1:n.482-15069G>T
ENST00000460319.5:n.508G>T
ENST00000466715.5:n.469G>T
ENST00000476070.1:n.488G>T
ENST00000479558.5:n.587G>T
ENST00000494398.5:n.589G>T
NM_001030311.2:c.589G>T	NP_001025482.1:p.Ala197Ser
NM_001030312.2:c.482-24069G>T	NP_001025483.1:n.482-24069G>T
NM_001030313.2:c.589G>T	NP_001025484.1:p.Ala197Ser
NM_001160277.1:c.482-7656G>T	NP_001153749.1:n.482-7656G>T
NM_201548.4:c.589G>T	NP_963842.1:p.Ala197Ser
NR_027689.1:n.583-15069G>T
NR_027690.1:n.690G>T
NM_201548.5:c.589G>T MANE Select	NP_963842.1:p.Ala197Ser
NM_001030311.3:c.589G>T	NP_001025482.1:p.Ala197Ser
NM_001030312.3:c.482-24069G>T	NP_001025483.1:n.482-24069G>T
NM_001030313.3:c.589G>T	NP_001025484.1:p.Ala197Ser
NM_001160277.2:c.482-7656G>T	NP_001153749.1:n.482-7656G>T
NR_027689.2:n.581-15069G>T
NR_027690.2:n.688G>T