Canonical Allele Identifier: CA693845771

Gene: CLECL1P

Linked Data

• dbSNP Id: rs1444388692
• gnomAD v3: 12-9723418-T-C
• gnomAD v4: 12-9723418-T-C
• MyVariant Identifiers: chr12:g.9876014T>C (hg19) ; chr12:g.9723418T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9723418T>C , CM000674.2:g.9723418T>C	GRCh38
NC_000012.11:g.9876014T>C , CM000674.1:g.9876014T>C	GRCh37
NC_000012.10:g.9767281T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000702603.1:n.150-605A>G
ENST00000327839.4:n.352-605A>G
ENST00000621400.5:n.263-605A>G
ENST00000327839.3:c.317-605A>G	ENSP00000331766.3:n.317-605A>G
ENST00000542530.5:c.172-605A>G
ENST00000621400.4:c.317-605A>G	ENSP00000483624.1:n.317-605A>G
NM_001253750.1:c.317-605A>G	NP_001240679.1:n.317-605A>G
NM_001267701.1:c.317-605A>G	NP_001254630.1:n.317-605A>G
NM_172004.3:c.317-605A>G	NP_742001.1:n.317-605A>G
XM_011520574.1:c.317-605A>G	XP_011518876.1:n.317-605A>G
XM_011520574.2:c.317-605A>G	XP_011518876.1:n.317-605A>G
XM_017018885.1:c.149-605A>G	XP_016874374.1:n.149-605A>G
NR_172485.1:n.349-605A>G
NR_172486.1:n.349-605A>G