Canonical Allele Identifier: CA430407610

Gene: CERKL

Linked Data

• MyVariant Identifiers: chr2:g.182423297T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558570T>G , CM000664.2:g.181558570T>G	GRCh38
NC_000002.11:g.182423297T>G , CM000664.1:g.182423297T>G	GRCh37
NC_000002.10:g.182131542T>G	NCBI36
NG_021178.1:g.103538A>C
NG_021178.2:g.103538A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.60A>C	ENSP00000508396.1:p.Pro20=
ENST00000410087.8:c.816A>C MANE Select	ENSP00000386725.3:p.Pro272=
ENST00000339098.9:c.894A>C	ENSP00000341159.5:p.Pro298=
ENST00000374967.6:c.752A>C	ENSP00000364106.2:n.752A>C
ENST00000374969.6:c.482-8862A>C	ENSP00000364108.2:n.482-8862A>C
ENST00000374970.6:c.614-8862A>C	ENSP00000364109.2:n.614-8862A>C
ENST00000409440.7:c.762A>C	ENSP00000387080.3:p.Pro254=
ENST00000410087.7:c.816A>C	ENSP00000386725.3:p.Pro272=
ENST00000421817.5:c.*98A>C	ENSP00000411466.1:n.*98A>C
ENST00000452174.5:c.620A>C	ENSP00000409198.1:n.620A>C
ENST00000479558.5:n.814A>C
ENST00000494398.5:n.816A>C
NM_001030311.2:c.894A>C	NP_001025482.1:p.Pro298=
NM_001030312.2:c.482-8862A>C	NP_001025483.1:n.482-8862A>C
NM_001030313.2:c.614-8862A>C	NP_001025484.1:n.614-8862A>C
NM_001160277.1:c.762A>C	NP_001153749.1:p.Pro254=
NM_201548.4:c.816A>C	NP_963842.1:p.Pro272=
NR_027689.1:n.721A>C
NR_027690.1:n.853A>C
NM_201548.5:c.816A>C MANE Select	NP_963842.1:p.Pro272=
NM_001030311.3:c.894A>C	NP_001025482.1:p.Pro298=
NM_001030312.3:c.482-8862A>C	NP_001025483.1:n.482-8862A>C
NM_001030313.3:c.614-8862A>C	NP_001025484.1:n.614-8862A>C
NM_001160277.2:c.762A>C	NP_001153749.1:p.Pro254=
NR_027689.2:n.719A>C
NR_027690.2:n.851A>C