Canonical Allele Identifier: CA1410105629

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186973_149186974delinsGC , CM000665.2:g.149186973_149186974delinsGC	GRCh38
NC_000003.11:g.148904760_148904761delinsGC , CM000665.1:g.148904760_148904761delinsGC	GRCh37
NC_000003.10:g.150387450_150387451delinsGC	NCBI36
NG_011800.1:g.40072_40073delinsGC
NG_011800.2:g.40072_40073delinsGC
NG_011800.3:g.40072_40073delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.1865-242_1865-241delinsGC MANE Select	ENSP00000264613.6:n.1865-242_1865-241delinsGC
ENST00000264613.10:c.1865-242_1865-241delinsGC	ENSP00000264613.6:n.1865-242_1865-241delinsGC
ENST00000462336.5:n.239-242_239-241delinsGC
ENST00000481169.5:c.1864+1078_1864+1079delinsGC	ENSP00000418773.1:n.1864+1078_1864+1079delinsGC
ENST00000489736.5:n.1090-242_1090-241delinsGC
ENST00000490639.5:n.1897-242_1897-241delinsGC
ENST00000494544.1:c.1214-242_1214-241delinsGC	ENSP00000420545.1:n.1214-242_1214-241delinsGC
ENST00000497902.5:n.46-242_46-241delinsGC
NM_000096.3:c.1865-242_1865-241delinsGC	NP_000087.1:n.1865-242_1865-241delinsGC
NR_046371.1:n.2117+1078_2117+1079delinsGC
XM_006713499.2:c.1865-242_1865-241delinsGC	XP_006713562.1:n.1865-242_1865-241delinsGC
XM_006713500.2:c.1865-242_1865-241delinsGC	XP_006713563.1:n.1865-242_1865-241delinsGC
XM_006713501.2:c.1865-242_1865-241delinsGC	XP_006713564.1:n.1865-242_1865-241delinsGC
XM_006713502.2:c.1865-242_1865-241delinsGC	XP_006713565.1:n.1865-242_1865-241delinsGC
XM_011512435.1:c.1865-242_1865-241delinsGC	XP_011510737.1:n.1865-242_1865-241delinsGC
XR_427361.2:n.2123-242_2123-241delinsGC
XM_006713499.3:c.1865-242_1865-241delinsGC	XP_006713562.1:n.1865-242_1865-241delinsGC
XM_006713500.4:c.1865-242_1865-241delinsGC	XP_006713563.1:n.1865-242_1865-241delinsGC
XM_006713501.3:c.1865-242_1865-241delinsGC	XP_006713564.1:n.1865-242_1865-241delinsGC
XM_011512435.2:c.1865-242_1865-241delinsGC	XP_011510737.1:n.1865-242_1865-241delinsGC
XM_017005734.2:c.1865-242_1865-241delinsGC	XP_016861223.1:n.1865-242_1865-241delinsGC
XM_017005735.2:c.1865-242_1865-241delinsGC	XP_016861224.1:n.1865-242_1865-241delinsGC
XR_427361.3:n.2081-242_2081-241delinsGC
NM_000096.4:c.1865-242_1865-241delinsGC MANE Select	NP_000087.2:n.1865-242_1865-241delinsGC
NR_046371.2:n.1901+1078_1901+1079delinsGC