Canonical Allele Identifier: CA2662207521

Gene: CERKL

Linked Data

• gnomAD v4: 2-181558664-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.181558667del , CM000664.2:g.181558667del	GRCh38
NC_000002.11:g.182423394del , CM000664.1:g.182423394del	GRCh37
NC_000002.10:g.182131639del	NCBI36
NG_021178.1:g.103443del
NG_021178.2:g.103443del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684145.1:c.-36del	ENSP00000508396.1:n.-36del
ENST00000410087.8:c.721del MANE Select	ENSP00000386725.3:p.His241MetfsTer5
ENST00000339098.9:c.799del	ENSP00000341159.5:p.His267MetfsTer5
ENST00000374967.6:c.657del	ENSP00000364106.2:n.657del
ENST00000374969.6:c.482-8957del	ENSP00000364108.2:n.482-8957del
ENST00000374970.6:c.614-8957del	ENSP00000364109.2:n.614-8957del
ENST00000409440.7:c.667del	ENSP00000387080.3:p.His223MetfsTer5
ENST00000410087.7:c.721del	ENSP00000386725.3:p.His241MetfsTer5
ENST00000421817.5:c.*3del	ENSP00000411466.1:n.*3del
ENST00000452174.5:c.525del	ENSP00000409198.1:n.525del
ENST00000466715.5:n.537del
ENST00000479558.5:n.719del
ENST00000494398.5:n.721del
NM_001030311.2:c.799del	NP_001025482.1:p.His267MetfsTer5
NM_001030312.2:c.482-8957del	NP_001025483.1:n.482-8957del
NM_001030313.2:c.614-8957del	NP_001025484.1:n.614-8957del
NM_001160277.1:c.667del	NP_001153749.1:p.His223MetfsTer5
NM_201548.4:c.721del	NP_963842.1:p.His241MetfsTer5
NR_027689.1:n.626del
NR_027690.1:n.758del
NM_201548.5:c.721del MANE Select	NP_963842.1:p.His241MetfsTer5
NM_001030311.3:c.799del	NP_001025482.1:p.His267MetfsTer5
NM_001030312.3:c.482-8957del	NP_001025483.1:n.482-8957del
NM_001030313.3:c.614-8957del	NP_001025484.1:n.614-8957del
NM_001160277.2:c.667del	NP_001153749.1:p.His223MetfsTer5
NR_027689.2:n.624del
NR_027690.2:n.756del