Canonical Allele Identifier: CA2015616662
Gene: CLECL1P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.9723458A= , CM000674.2:g.9723458A= GRCh38
NC_000012.11:g.9876054A= , CM000674.1:g.9876054A= GRCh37
NC_000012.10:g.9767321A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000702603.1:n.150-645T=
ENST00000327839.4:n.352-645T=
ENST00000621400.5:n.263-645T=
ENST00000327839.3:c.317-645T= ENSP00000331766.3:n.317-645T=
ENST00000542530.5:c.172-645T=
ENST00000621400.4:c.317-645T= ENSP00000483624.1:n.317-645T=
NM_001253750.1:c.317-645T= NP_001240679.1:n.317-645T=
NM_001267701.1:c.317-645T= NP_001254630.1:n.317-645T=
NM_172004.3:c.317-645T= NP_742001.1:n.317-645T=
XM_011520574.1:c.317-645T= XP_011518876.1:n.317-645T=
XM_011520574.2:c.317-645T= XP_011518876.1:n.317-645T=
XM_017018885.1:c.149-645T= XP_016874374.1:n.149-645T=
NR_172485.1:n.349-645T=
NR_172486.1:n.349-645T=