Canonical Allele Identifier: CA693845992

Gene: CLECL1P

Linked Data

• dbSNP Id: rs1173715106
• gnomAD v3: 12-9723619-ACAT-A
• gnomAD v4: 12-9723619-ACAT-A
• MyVariant Identifiers: chr12:g.9876216_9876218del (hg19) ; chr12:g.9723620_9723622del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9723623_9723625del , CM000674.2:g.9723623_9723625del	GRCh38
NC_000012.11:g.9876219_9876221del , CM000674.1:g.9876219_9876221del	GRCh37
NC_000012.10:g.9767486_9767488del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000702603.1:n.150-809_150-807del
ENST00000327839.4:n.352-809_352-807del
ENST00000621400.5:n.263-809_263-807del
ENST00000327839.3:c.317-809_317-807del	ENSP00000331766.3:n.317-809_317-807del
ENST00000542530.5:c.172-809_172-807del
ENST00000621400.4:c.317-809_317-807del	ENSP00000483624.1:n.317-809_317-807del
NM_001253750.1:c.317-809_317-807del	NP_001240679.1:n.317-809_317-807del
NM_001267701.1:c.317-809_317-807del	NP_001254630.1:n.317-809_317-807del
NM_172004.3:c.317-809_317-807del	NP_742001.1:n.317-809_317-807del
XM_011520574.1:c.317-809_317-807del	XP_011518876.1:n.317-809_317-807del
XM_011520574.2:c.317-809_317-807del	XP_011518876.1:n.317-809_317-807del
XM_017018885.1:c.149-809_149-807del	XP_016874374.1:n.149-809_149-807del
NR_172485.1:n.349-809_349-807del
NR_172486.1:n.349-809_349-807del