Canonical Allele Identifier: CA603239401
Gene: CLECL1P HGNC NCBI

Linked Data

dbSNP Id: rs1180174984

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9723441_9723444del , CM000674.2:g.9723441_9723444del GRCh38
NC_000012.11:g.9876037_9876040del , CM000674.1:g.9876037_9876040del GRCh37
NC_000012.10:g.9767304_9767307del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000702603.1:n.150-622_150-619del
ENST00000327839.4:n.352-622_352-619del
ENST00000621400.5:n.263-622_263-619del
ENST00000327839.3:c.317-622_317-619del ENSP00000331766.3:n.317-622_317-619del
ENST00000542530.5:c.172-622_172-619del
ENST00000621400.4:c.317-622_317-619del ENSP00000483624.1:n.317-622_317-619del
NM_001253750.1:c.317-622_317-619del NP_001240679.1:n.317-622_317-619del
NM_001267701.1:c.317-622_317-619del NP_001254630.1:n.317-622_317-619del
NM_172004.3:c.317-622_317-619del NP_742001.1:n.317-622_317-619del
XM_011520574.1:c.317-622_317-619del XP_011518876.1:n.317-622_317-619del
XM_011520574.2:c.317-622_317-619del XP_011518876.1:n.317-622_317-619del
XM_017018885.1:c.149-622_149-619del XP_016874374.1:n.149-622_149-619del
NR_172485.1:n.349-622_349-619del
NR_172486.1:n.349-622_349-619del