Canonical Allele Identifier: CA232729397

Gene: CLECL1P

Linked Data

• dbSNP Id: rs61508153
• gnomAD v2: 12-9876037-GACAC-G
• gnomAD v3: 12-9723441-GACAC-G
• gnomAD v4: 12-9723441-GACAC-G
• MyVariant Identifiers: chr12:g.9876040_9876043del (hg19) ; chr12:g.9876038_9876041del (hg19) ; chr12:g.9723444_9723447del (hg38) ; chr12:g.9723442_9723445del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.9723456_9723459del , CM000674.2:g.9723456_9723459del	GRCh38
NC_000012.11:g.9876052_9876055del , CM000674.1:g.9876052_9876055del	GRCh37
NC_000012.10:g.9767319_9767322del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000702603.1:n.150-632_150-629del
ENST00000327839.4:n.352-632_352-629del
ENST00000621400.5:n.263-632_263-629del
ENST00000327839.3:c.317-632_317-629del	ENSP00000331766.3:n.317-632_317-629del
ENST00000542530.5:c.172-632_172-629del
ENST00000621400.4:c.317-632_317-629del	ENSP00000483624.1:n.317-632_317-629del
NM_001253750.1:c.317-632_317-629del	NP_001240679.1:n.317-632_317-629del
NM_001267701.1:c.317-632_317-629del	NP_001254630.1:n.317-632_317-629del
NM_172004.3:c.317-632_317-629del	NP_742001.1:n.317-632_317-629del
XM_011520574.1:c.317-632_317-629del	XP_011518876.1:n.317-632_317-629del
XM_011520574.2:c.317-632_317-629del	XP_011518876.1:n.317-632_317-629del
XM_017018885.1:c.149-632_149-629del	XP_016874374.1:n.149-632_149-629del
NR_172485.1:n.349-632_349-629del
NR_172486.1:n.349-632_349-629del