Canonical Allele Identifier: CA61617148
Gene: CERKL HGNC NCBI

Linked Data

dbSNP Id: rs993648

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181591267C>T , CM000664.2:g.181591267C>T GRCh38
NC_000002.11:g.182455994C>T , CM000664.1:g.182455994C>T GRCh37
NC_000002.10:g.182164239C>T NCBI36
NG_021178.1:g.70841G>A
NG_021178.2:g.70841G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684145.1:c.-212+12570G>A ENSP00000508396.1:n.-212+12570G>A
ENST00000410087.8:c.481+12570G>A MANE Select ENSP00000386725.3:n.481+12570G>A
ENST00000339098.9:c.481+12570G>A ENSP00000341159.5:n.481+12570G>A
ENST00000374967.6:c.481+12570G>A ENSP00000364106.2:n.481+12570G>A
ENST00000374969.6:c.481+12570G>A ENSP00000364108.2:n.481+12570G>A
ENST00000374970.6:c.481+12570G>A ENSP00000364109.2:n.481+12570G>A
ENST00000409440.7:c.481+12570G>A ENSP00000387080.3:n.481+12570G>A
ENST00000410087.7:c.481+12570G>A ENSP00000386725.3:n.481+12570G>A
ENST00000421817.5:c.481+12570G>A ENSP00000411466.1:n.481+12570G>A
ENST00000452174.5:c.481+12570G>A ENSP00000409198.1:n.481+12570G>A
ENST00000460319.5:n.400+12570G>A
ENST00000466715.5:n.361+12570G>A
ENST00000476070.1:n.380+12570G>A
ENST00000479558.5:n.479+12570G>A
ENST00000494398.5:n.481+12570G>A
NM_001030311.2:c.481+12570G>A NP_001025482.1:n.481+12570G>A
NM_001030312.2:c.481+12570G>A NP_001025483.1:n.481+12570G>A
NM_001030313.2:c.481+12570G>A NP_001025484.1:n.481+12570G>A
NM_001160277.1:c.481+12570G>A NP_001153749.1:n.481+12570G>A
NM_201548.4:c.481+12570G>A NP_963842.1:n.481+12570G>A
NR_027689.1:n.582+12570G>A
NR_027690.1:n.582+12570G>A
NM_201548.5:c.481+12570G>A MANE Select NP_963842.1:n.481+12570G>A
NM_001030311.3:c.481+12570G>A NP_001025482.1:n.481+12570G>A
NM_001030312.3:c.481+12570G>A NP_001025483.1:n.481+12570G>A
NM_001030313.3:c.481+12570G>A NP_001025484.1:n.481+12570G>A
NM_001160277.2:c.481+12570G>A NP_001153749.1:n.481+12570G>A
NR_027689.2:n.580+12570G>A
NR_027690.2:n.580+12570G>A