Canonical Allele Identifier: CA547366015

Gene: CP

Linked Data

• dbSNP Id: rs1448181546
• gnomAD v2: 3-148904696-AG-A
• gnomAD v3: 3-149186909-AG-A
• gnomAD v4: 3-149186909-AG-A
• MyVariant Identifiers: chr3:g.148904697del (hg19) ; chr3:g.149186910del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186910del , CM000665.2:g.149186910del	GRCh38
NC_000003.11:g.148904697del , CM000665.1:g.148904697del	GRCh37
NC_000003.10:g.150387387del	NCBI36
NG_011800.1:g.40136del
NG_011800.2:g.40136del
NG_011800.3:g.40136del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.1865-178del MANE Select	ENSP00000264613.6:n.1865-178del
ENST00000264613.10:c.1865-178del	ENSP00000264613.6:n.1865-178del
ENST00000462336.5:n.239-178del
ENST00000481169.5:c.1864+1142del	ENSP00000418773.1:n.1864+1142del
ENST00000489736.5:n.1090-178del
ENST00000490639.5:n.1897-178del
ENST00000494544.1:c.1214-178del	ENSP00000420545.1:n.1214-178del
ENST00000497902.5:n.46-178del
NM_000096.3:c.1865-178del	NP_000087.1:n.1865-178del
NR_046371.1:n.2117+1142del
XM_006713499.2:c.1865-178del	XP_006713562.1:n.1865-178del
XM_006713500.2:c.1865-178del	XP_006713563.1:n.1865-178del
XM_006713501.2:c.1865-178del	XP_006713564.1:n.1865-178del
XM_006713502.2:c.1865-178del	XP_006713565.1:n.1865-178del
XM_011512435.1:c.1865-178del	XP_011510737.1:n.1865-178del
XR_427361.2:n.2123-178del
XM_006713499.3:c.1865-178del	XP_006713562.1:n.1865-178del
XM_006713500.4:c.1865-178del	XP_006713563.1:n.1865-178del
XM_006713501.3:c.1865-178del	XP_006713564.1:n.1865-178del
XM_011512435.2:c.1865-178del	XP_011510737.1:n.1865-178del
XM_017005734.2:c.1865-178del	XP_016861223.1:n.1865-178del
XM_017005735.2:c.1865-178del	XP_016861224.1:n.1865-178del
XR_427361.3:n.2081-178del
NM_000096.4:c.1865-178del MANE Select	NP_000087.2:n.1865-178del
NR_046371.2:n.1901+1142del