Canonical Allele Identifier: CA2577178397

Gene: CERKL

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181573701del , CM000664.2:g.181573701del	GRCh38
NC_000002.11:g.182438428del , CM000664.1:g.182438428del	GRCh37
NC_000002.10:g.182146673del	NCBI36
NG_021178.1:g.88410del
NG_021178.2:g.88410del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-80+55del	ENSP00000508396.1:n.-80+55del
ENST00000410087.8:c.613+55del MANE Select	ENSP00000386725.3:n.613+55del
ENST00000339098.9:c.613+55del	ENSP00000341159.5:n.613+55del
ENST00000374967.6:c.613+55del	ENSP00000364106.2:n.613+55del
ENST00000374969.6:c.482-23990del	ENSP00000364108.2:n.482-23990del
ENST00000374970.6:c.613+55del	ENSP00000364109.2:n.613+55del
ENST00000409440.7:c.482-7577del	ENSP00000387080.3:n.482-7577del
ENST00000410087.7:c.613+55del	ENSP00000386725.3:n.613+55del
ENST00000421817.5:c.482-14990del	ENSP00000411466.1:n.482-14990del
ENST00000452174.5:c.482-14990del	ENSP00000409198.1:n.482-14990del
ENST00000460319.5:n.532+55del
ENST00000466715.5:n.493+55del
ENST00000476070.1:n.512+55del
ENST00000479558.5:n.611+55del
ENST00000494398.5:n.613+55del
NM_001030311.2:c.613+55del	NP_001025482.1:n.613+55del
NM_001030312.2:c.482-23990del	NP_001025483.1:n.482-23990del
NM_001030313.2:c.613+55del	NP_001025484.1:n.613+55del
NM_001160277.1:c.482-7577del	NP_001153749.1:n.482-7577del
NM_201548.4:c.613+55del	NP_963842.1:n.613+55del
NR_027689.1:n.583-14990del
NR_027690.1:n.714+55del
NM_201548.5:c.613+55del MANE Select	NP_963842.1:n.613+55del
NM_001030311.3:c.613+55del	NP_001025482.1:n.613+55del
NM_001030312.3:c.482-23990del	NP_001025483.1:n.482-23990del
NM_001030313.3:c.613+55del	NP_001025484.1:n.613+55del
NM_001160277.2:c.482-7577del	NP_001153749.1:n.482-7577del
NR_027689.2:n.581-14990del
NR_027690.2:n.712+55del