Canonical Allele Identifier: CA2507422157

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186454_149186455insACCTAAACTTTTCATCATGTCTCTGTAGCCTAGATGTAGTGTTGG , CM000665.2:g.149186454_149186455insACCTAAACTTTTCATCATGTCTCTGTAGCCTAGATGTAGTGTTGG	GRCh38
NC_000003.11:g.148904241_148904242insACCTAAACTTTTCATCATGTCTCTGTAGCCTAGATGTAGTGTTGG , CM000665.1:g.148904241_148904242insACCTAAACTTTTCATCATGTCTCTGTAGCCTAGATGTAGTGTTGG	GRCh37
NC_000003.10:g.150386931_150386932insACCTAAACTTTTCATCATGTCTCTGTAGCCTAGATGTAGTGTTGG	NCBI36
NG_011800.1:g.40591_40592insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT
NG_011800.2:g.40591_40592insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT
NG_011800.3:g.40591_40592insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT MANE Select	ENSP00000264613.6:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAG...
ENST00000264613.10:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	ENSP00000264613.6:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAG...
ENST00000462336.5:n.451+65_451+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT
ENST00000481169.5:c.1865-1009_1865-1008insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	ENSP00000418773.1:n.1865-1009_1865-1008insCCAACACTACATCTAGGCT...
ENST00000489736.5:n.1367_1368insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT
ENST00000490639.5:n.2109+65_2109+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT
ENST00000494544.1:c.1426+65_1426+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	ENSP00000420545.1:n.1426+65_1426+66insCCAACACTACATCTAGGCTACAG...
ENST00000497902.5:n.258+65_258+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT
NM_000096.3:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	NP_000087.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACAT...
NR_046371.1:n.2118-1009_2118-1008insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT
XM_006713499.2:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_006713562.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XM_006713500.2:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_006713563.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XM_006713501.2:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_006713564.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XM_006713502.2:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_006713565.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XM_011512435.1:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_011510737.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XR_427361.2:n.2335+65_2335+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT
XM_006713499.3:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_006713562.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XM_006713500.4:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_006713563.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XM_006713501.3:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_006713564.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XM_011512435.2:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_011510737.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XM_017005734.2:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_016861223.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XM_017005735.2:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT	XP_016861224.1:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGA...
XR_427361.3:n.2293+65_2293+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT
NM_000096.4:c.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT MANE Select	NP_000087.2:n.2077+65_2077+66insCCAACACTACATCTAGGCTACAGAGACAT...
NR_046371.2:n.1902-1009_1902-1008insCCAACACTACATCTAGGCTACAGAGACATGATGAAAAGTTTAGGT