Canonical Allele Identifier: CA2830535515

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186975_149186976insTAGA , CM000665.2:g.149186975_149186976insTAGA	GRCh38
NC_000003.11:g.148904762_148904763insTAGA , CM000665.1:g.148904762_148904763insTAGA	GRCh37
NC_000003.10:g.150387452_150387453insTAGA	NCBI36
NG_011800.1:g.40071_40072insCTAT
NG_011800.2:g.40071_40072insCTAT
NG_011800.3:g.40071_40072insCTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.1865-243_1865-242insCTAT MANE Select	ENSP00000264613.6:n.1865-243_1865-242insCTAT
ENST00000264613.10:c.1865-243_1865-242insCTAT	ENSP00000264613.6:n.1865-243_1865-242insCTAT
ENST00000462336.5:n.239-243_239-242insCTAT
ENST00000481169.5:c.1864+1077_1864+1078insCTAT	ENSP00000418773.1:n.1864+1077_1864+1078insCTAT
ENST00000489736.5:n.1090-243_1090-242insCTAT
ENST00000490639.5:n.1897-243_1897-242insCTAT
ENST00000494544.1:c.1214-243_1214-242insCTAT	ENSP00000420545.1:n.1214-243_1214-242insCTAT
ENST00000497902.5:n.46-243_46-242insCTAT
NM_000096.3:c.1865-243_1865-242insCTAT	NP_000087.1:n.1865-243_1865-242insCTAT
NR_046371.1:n.2117+1077_2117+1078insCTAT
XM_006713499.2:c.1865-243_1865-242insCTAT	XP_006713562.1:n.1865-243_1865-242insCTAT
XM_006713500.2:c.1865-243_1865-242insCTAT	XP_006713563.1:n.1865-243_1865-242insCTAT
XM_006713501.2:c.1865-243_1865-242insCTAT	XP_006713564.1:n.1865-243_1865-242insCTAT
XM_006713502.2:c.1865-243_1865-242insCTAT	XP_006713565.1:n.1865-243_1865-242insCTAT
XM_011512435.1:c.1865-243_1865-242insCTAT	XP_011510737.1:n.1865-243_1865-242insCTAT
XR_427361.2:n.2123-243_2123-242insCTAT
XM_006713499.3:c.1865-243_1865-242insCTAT	XP_006713562.1:n.1865-243_1865-242insCTAT
XM_006713500.4:c.1865-243_1865-242insCTAT	XP_006713563.1:n.1865-243_1865-242insCTAT
XM_006713501.3:c.1865-243_1865-242insCTAT	XP_006713564.1:n.1865-243_1865-242insCTAT
XM_011512435.2:c.1865-243_1865-242insCTAT	XP_011510737.1:n.1865-243_1865-242insCTAT
XM_017005734.2:c.1865-243_1865-242insCTAT	XP_016861223.1:n.1865-243_1865-242insCTAT
XM_017005735.2:c.1865-243_1865-242insCTAT	XP_016861224.1:n.1865-243_1865-242insCTAT
XR_427361.3:n.2081-243_2081-242insCTAT
NM_000096.4:c.1865-243_1865-242insCTAT MANE Select	NP_000087.2:n.1865-243_1865-242insCTAT
NR_046371.2:n.1901+1077_1901+1078insCTAT