Canonical Allele Identifier: CA349740302

Gene: CERKL

Linked Data

• MyVariant Identifiers: chr2:g.182423334G>T (hg19) ; chr2:g.181558607G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558607G>T , CM000664.2:g.181558607G>T	GRCh38
NC_000002.11:g.182423334G>T , CM000664.1:g.182423334G>T	GRCh37
NC_000002.10:g.182131579G>T	NCBI36
NG_021178.1:g.103501C>A
NG_021178.2:g.103501C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.23C>A	ENSP00000508396.1:p.Thr8Asn
ENST00000410087.8:c.779C>A MANE Select	ENSP00000386725.3:p.Thr260Asn
ENST00000339098.9:c.857C>A	ENSP00000341159.5:p.Thr286Asn
ENST00000374967.6:c.715C>A	ENSP00000364106.2:n.715C>A
ENST00000374969.6:c.482-8899C>A	ENSP00000364108.2:n.482-8899C>A
ENST00000374970.6:c.614-8899C>A	ENSP00000364109.2:n.614-8899C>A
ENST00000409440.7:c.725C>A	ENSP00000387080.3:p.Thr242Asn
ENST00000410087.7:c.779C>A	ENSP00000386725.3:p.Thr260Asn
ENST00000421817.5:c.*61C>A	ENSP00000411466.1:n.*61C>A
ENST00000452174.5:c.583C>A	ENSP00000409198.1:n.583C>A
ENST00000479558.5:n.777C>A
ENST00000494398.5:n.779C>A
NM_001030311.2:c.857C>A	NP_001025482.1:p.Thr286Asn
NM_001030312.2:c.482-8899C>A	NP_001025483.1:n.482-8899C>A
NM_001030313.2:c.614-8899C>A	NP_001025484.1:n.614-8899C>A
NM_001160277.1:c.725C>A	NP_001153749.1:p.Thr242Asn
NM_201548.4:c.779C>A	NP_963842.1:p.Thr260Asn
NR_027689.1:n.684C>A
NR_027690.1:n.816C>A
NM_201548.5:c.779C>A MANE Select	NP_963842.1:p.Thr260Asn
NM_001030311.3:c.857C>A	NP_001025482.1:p.Thr286Asn
NM_001030312.3:c.482-8899C>A	NP_001025483.1:n.482-8899C>A
NM_001030313.3:c.614-8899C>A	NP_001025484.1:n.614-8899C>A
NM_001160277.2:c.725C>A	NP_001153749.1:p.Thr242Asn
NR_027689.2:n.682C>A
NR_027690.2:n.814C>A