Canonical Allele Identifier: CA1410105348

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186633_149186639delinsACATCGG , CM000665.2:g.149186633_149186639delinsACATCGG	GRCh38
NC_000003.11:g.148904420_148904426delinsACATCGG , CM000665.1:g.148904420_148904426delinsACATCGG	GRCh37
NC_000003.10:g.150387110_150387116delinsACATCGG	NCBI36
NG_011800.1:g.40407_40413delinsCCGATGT
NG_011800.2:g.40407_40413delinsCCGATGT
NG_011800.3:g.40407_40413delinsCCGATGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.1958_1964delinsCCGATGT MANE Select	ENSP00000264613.6:p.Ala653=
ENST00000264613.10:c.1958_1964delinsCCGATGT	ENSP00000264613.6:p.Ala653=
ENST00000462336.5:n.332_338delinsCCGATGT
ENST00000481169.5:c.1865-1193_1865-1187delinsCCGATGT	ENSP00000418773.1:n.1865-1193_1865-1187de...
ENST00000489736.5:n.1183_1189delinsCCGATGT
ENST00000490639.5:n.1990_1996delinsCCGATGT
ENST00000494544.1:c.1307_1313delinsCCGATGT	ENSP00000420545.1:p.Ala436=
ENST00000497902.5:n.139_145delinsCCGATGT
NM_000096.3:c.1958_1964delinsCCGATGT	NP_000087.1:p.Ala653=
NR_046371.1:n.2118-1193_2118-1187delinsCCGATGT
XM_006713499.2:c.1958_1964delinsCCGATGT	XP_006713562.1:p.Ala653=
XM_006713500.2:c.1958_1964delinsCCGATGT	XP_006713563.1:p.Ala653=
XM_006713501.2:c.1958_1964delinsCCGATGT	XP_006713564.1:p.Ala653=
XM_006713502.2:c.1958_1964delinsCCGATGT	XP_006713565.1:p.Ala653=
XM_011512435.1:c.1958_1964delinsCCGATGT	XP_011510737.1:p.Ala653=
XR_427361.2:n.2216_2222delinsCCGATGT
XM_006713499.3:c.1958_1964delinsCCGATGT	XP_006713562.1:p.Ala653=
XM_006713500.4:c.1958_1964delinsCCGATGT	XP_006713563.1:p.Ala653=
XM_006713501.3:c.1958_1964delinsCCGATGT	XP_006713564.1:p.Ala653=
XM_011512435.2:c.1958_1964delinsCCGATGT	XP_011510737.1:p.Ala653=
XM_017005734.2:c.1958_1964delinsCCGATGT	XP_016861223.1:p.Ala653=
XM_017005735.2:c.1958_1964delinsCCGATGT	XP_016861224.1:p.Ala653=
XR_427361.3:n.2174_2180delinsCCGATGT
NM_000096.4:c.1958_1964delinsCCGATGT MANE Select	NP_000087.2:p.Ala653=
NR_046371.2:n.1902-1193_1902-1187delinsCCGATGT