Canonical Allele Identifier: CA693846001

Gene: CLECL1P

Linked Data

• dbSNP Id: rs1421517310
• gnomAD v3: 12-9723633-CCT-C
• gnomAD v4: 12-9723633-CCT-C
• MyVariant Identifiers: chr12:g.9876230_9876231del (hg19) ; chr12:g.9723634_9723635del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9723634_9723635del , CM000674.2:g.9723634_9723635del	GRCh38
NC_000012.11:g.9876230_9876231del , CM000674.1:g.9876230_9876231del	GRCh37
NC_000012.10:g.9767497_9767498del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000702603.1:n.150-822_150-821del
ENST00000327839.4:n.352-822_352-821del
ENST00000621400.5:n.263-822_263-821del
ENST00000327839.3:c.317-822_317-821del	ENSP00000331766.3:n.317-822_317-821del
ENST00000542530.5:c.172-822_172-821del
ENST00000621400.4:c.317-822_317-821del	ENSP00000483624.1:n.317-822_317-821del
NM_001253750.1:c.317-822_317-821del	NP_001240679.1:n.317-822_317-821del
NM_001267701.1:c.317-822_317-821del	NP_001254630.1:n.317-822_317-821del
NM_172004.3:c.317-822_317-821del	NP_742001.1:n.317-822_317-821del
XM_011520574.1:c.317-822_317-821del	XP_011518876.1:n.317-822_317-821del
XM_011520574.2:c.317-822_317-821del	XP_011518876.1:n.317-822_317-821del
XM_017018885.1:c.149-822_149-821del	XP_016874374.1:n.149-822_149-821del
NR_172485.1:n.349-822_349-821del
NR_172486.1:n.349-822_349-821del