Canonical Allele Identifier: CA239056

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181656941G>C , CM000664.2:g.181656941G>C	GRCh38
NC_000002.11:g.182521668G>C , CM000664.1:g.182521668G>C	GRCh37
NC_000002.10:g.182229913G>C	NCBI36
NG_021178.1:g.5167C>G
NG_021178.2:g.5167C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-455+23489C>G	ENSP00000508396.1:n.-455+23489C>G
ENST00000410087.8:c.66C>G MANE Select	ENSP00000386725.3:p.Pro22=
ENST00000339098.9:c.66C>G	ENSP00000341159.5:p.Pro22=
ENST00000374967.6:c.66C>G	ENSP00000364106.2:p.Pro22=
ENST00000374969.6:c.66C>G	ENSP00000364108.2:p.Pro22=
ENST00000374970.6:c.66C>G	ENSP00000364109.2:p.Pro22=
ENST00000409440.7:c.66C>G	ENSP00000387080.3:p.Pro22=
ENST00000410087.7:c.66C>G	ENSP00000386725.3:p.Pro22=
ENST00000421817.5:c.66C>G	ENSP00000411466.1:p.Pro22=
ENST00000452174.5:c.66C>G	ENSP00000409198.1:p.Pro22=
ENST00000476070.1:n.137+39C>G
ENST00000479558.5:n.236+23489C>G
ENST00000494398.5:n.66C>G
ENST00000497337.1:n.212+23489C>G
NM_001030311.2:c.66C>G	NP_001025482.1:p.Pro22=
NM_001030312.2:c.66C>G	NP_001025483.1:p.Pro22=
NM_001030313.2:c.66C>G	NP_001025484.1:p.Pro22=
NM_001160277.1:c.66C>G	NP_001153749.1:p.Pro22=
NM_201548.4:c.66C>G	NP_963842.1:p.Pro22=
NR_027689.1:n.167C>G
NR_027690.1:n.167C>G
NM_201548.5:c.66C>G MANE Select	NP_963842.1:p.Pro22=
NM_001030311.3:c.66C>G	NP_001025482.1:p.Pro22=
NM_001030312.3:c.66C>G	NP_001025483.1:p.Pro22=
NM_001030313.3:c.66C>G	NP_001025484.1:p.Pro22=
NM_001160277.2:c.66C>G	NP_001153749.1:p.Pro22=
NR_027689.2:n.165C>G
NR_027690.2:n.165C>G