Canonical Allele Identifier: CA2586970896
Gene: CERKL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.181558670_181558671dup , CM000664.2:g.181558670_181558671dup GRCh38
NC_000002.11:g.182423397_182423398dup , CM000664.1:g.182423397_182423398dup GRCh37
NC_000002.10:g.182131642_182131643dup NCBI36
NG_021178.1:g.103437_103438dup
NG_021178.2:g.103437_103438dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684145.1:c.-42_-41dup ENSP00000508396.1:n.-42_-41dup
ENST00000410087.8:c.715_716dup MANE Select ENSP00000386725.3:p.Ala240Ter
ENST00000339098.9:c.793_794dup ENSP00000341159.5:p.Ala266Ter
ENST00000374967.6:c.651_652dup ENSP00000364106.2:p.Ter218CysextTer?
ENST00000374969.6:c.482-8963_482-8962dup ENSP00000364108.2:n.482-8963_482-8962dup
ENST00000374970.6:c.614-8963_614-8962dup ENSP00000364109.2:n.614-8963_614-8962dup
ENST00000409440.7:c.661_662dup ENSP00000387080.3:p.Ala222Ter
ENST00000410087.7:c.715_716dup ENSP00000386725.3:p.Ala240Ter
ENST00000421817.5:c.519_520dup ENSP00000411466.1:p.Ter174CysextTer?
ENST00000452174.5:c.519_520dup ENSP00000409198.1:p.Ter174CysextTer?
ENST00000466715.5:n.531_532dup
ENST00000479558.5:n.713_714dup
ENST00000494398.5:n.715_716dup
NM_001030311.2:c.793_794dup NP_001025482.1:p.Ala266Ter
NM_001030312.2:c.482-8963_482-8962dup NP_001025483.1:n.482-8963_482-8962dup
NM_001030313.2:c.614-8963_614-8962dup NP_001025484.1:n.614-8963_614-8962dup
NM_001160277.1:c.661_662dup NP_001153749.1:p.Ala222Ter
NM_201548.4:c.715_716dup NP_963842.1:p.Ala240Ter
NR_027689.1:n.620_621dup
NR_027690.1:n.752_753dup
NM_201548.5:c.715_716dup MANE Select NP_963842.1:p.Ala240Ter
NM_001030311.3:c.793_794dup NP_001025482.1:p.Ala266Ter
NM_001030312.3:c.482-8963_482-8962dup NP_001025483.1:n.482-8963_482-8962dup
NM_001030313.3:c.614-8963_614-8962dup NP_001025484.1:n.614-8963_614-8962dup
NM_001160277.2:c.661_662dup NP_001153749.1:p.Ala222Ter
NR_027689.2:n.618_619dup
NR_027690.2:n.750_751dup