Canonical Allele Identifier: CA1410105096

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186458_149186459delinsAG , CM000665.2:g.149186458_149186459delinsAG	GRCh38
NC_000003.11:g.148904245_148904246delinsAG , CM000665.1:g.148904245_148904246delinsAG	GRCh37
NC_000003.10:g.150386935_150386936delinsAG	NCBI36
NG_011800.1:g.40587_40588delinsCT
NG_011800.2:g.40587_40588delinsCT
NG_011800.3:g.40587_40588delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2077+61_2077+62delinsCT MANE Select	ENSP00000264613.6:n.2077+61_2077+62delinsCT
ENST00000264613.10:c.2077+61_2077+62delinsCT	ENSP00000264613.6:n.2077+61_2077+62delinsCT
ENST00000462336.5:n.451+61_451+62delinsCT
ENST00000481169.5:c.1865-1013_1865-1012delinsCT	ENSP00000418773.1:n.1865-1013_1865-1012delinsCT
ENST00000489736.5:n.1363_1364delinsCT
ENST00000490639.5:n.2109+61_2109+62delinsCT
ENST00000494544.1:c.1426+61_1426+62delinsCT	ENSP00000420545.1:n.1426+61_1426+62delinsCT
ENST00000497902.5:n.258+61_258+62delinsCT
NM_000096.3:c.2077+61_2077+62delinsCT	NP_000087.1:n.2077+61_2077+62delinsCT
NR_046371.1:n.2118-1013_2118-1012delinsCT
XM_006713499.2:c.2077+61_2077+62delinsCT	XP_006713562.1:n.2077+61_2077+62delinsCT
XM_006713500.2:c.2077+61_2077+62delinsCT	XP_006713563.1:n.2077+61_2077+62delinsCT
XM_006713501.2:c.2077+61_2077+62delinsCT	XP_006713564.1:n.2077+61_2077+62delinsCT
XM_006713502.2:c.2077+61_2077+62delinsCT	XP_006713565.1:n.2077+61_2077+62delinsCT
XM_011512435.1:c.2077+61_2077+62delinsCT	XP_011510737.1:n.2077+61_2077+62delinsCT
XR_427361.2:n.2335+61_2335+62delinsCT
XM_006713499.3:c.2077+61_2077+62delinsCT	XP_006713562.1:n.2077+61_2077+62delinsCT
XM_006713500.4:c.2077+61_2077+62delinsCT	XP_006713563.1:n.2077+61_2077+62delinsCT
XM_006713501.3:c.2077+61_2077+62delinsCT	XP_006713564.1:n.2077+61_2077+62delinsCT
XM_011512435.2:c.2077+61_2077+62delinsCT	XP_011510737.1:n.2077+61_2077+62delinsCT
XM_017005734.2:c.2077+61_2077+62delinsCT	XP_016861223.1:n.2077+61_2077+62delinsCT
XM_017005735.2:c.2077+61_2077+62delinsCT	XP_016861224.1:n.2077+61_2077+62delinsCT
XR_427361.3:n.2293+61_2293+62delinsCT
NM_000096.4:c.2077+61_2077+62delinsCT MANE Select	NP_000087.2:n.2077+61_2077+62delinsCT
NR_046371.2:n.1902-1013_1902-1012delinsCT