Canonical Allele Identifier: CA2758855870

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186122_149186123insGGTGG , CM000665.2:g.149186122_149186123insGGTGG	GRCh38
NC_000003.11:g.148903909_148903910insGGTGG , CM000665.1:g.148903909_148903910insGGTGG	GRCh37
NC_000003.10:g.150386599_150386600insGGTGG	NCBI36
NG_011800.1:g.40923_40924insCCACC
NG_011800.2:g.40923_40924insCCACC
NG_011800.3:g.40923_40924insCCACC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2077+397_2077+398insCCACC MANE Select	ENSP00000264613.6:n.2077+397_2077+398insCCACC
ENST00000264613.10:c.2077+397_2077+398insCCACC	ENSP00000264613.6:n.2077+397_2077+398insCCACC
ENST00000462336.5:n.451+397_451+398insCCACC
ENST00000481169.5:c.1865-677_1865-676insCCACC	ENSP00000418773.1:n.1865-677_1865-676insCCACC
ENST00000489736.5:n.1699_1700insCCACC
ENST00000490639.5:n.2109+397_2109+398insCCACC
ENST00000494544.1:c.1426+397_1426+398insCCACC	ENSP00000420545.1:n.1426+397_1426+398insCCACC
ENST00000497902.5:n.258+397_258+398insCCACC
NM_000096.3:c.2077+397_2077+398insCCACC	NP_000087.1:n.2077+397_2077+398insCCACC
NR_046371.1:n.2118-677_2118-676insCCACC
XM_006713499.2:c.2077+397_2077+398insCCACC	XP_006713562.1:n.2077+397_2077+398insCCACC
XM_006713500.2:c.2077+397_2077+398insCCACC	XP_006713563.1:n.2077+397_2077+398insCCACC
XM_006713501.2:c.2077+397_2077+398insCCACC	XP_006713564.1:n.2077+397_2077+398insCCACC
XM_006713502.2:c.2077+397_2077+398insCCACC	XP_006713565.1:n.2077+397_2077+398insCCACC
XM_011512435.1:c.2077+397_2077+398insCCACC	XP_011510737.1:n.2077+397_2077+398insCCACC
XR_427361.2:n.2335+397_2335+398insCCACC
XM_006713499.3:c.2077+397_2077+398insCCACC	XP_006713562.1:n.2077+397_2077+398insCCACC
XM_006713500.4:c.2077+397_2077+398insCCACC	XP_006713563.1:n.2077+397_2077+398insCCACC
XM_006713501.3:c.2077+397_2077+398insCCACC	XP_006713564.1:n.2077+397_2077+398insCCACC
XM_011512435.2:c.2077+397_2077+398insCCACC	XP_011510737.1:n.2077+397_2077+398insCCACC
XM_017005734.2:c.2077+397_2077+398insCCACC	XP_016861223.1:n.2077+397_2077+398insCCACC
XM_017005735.2:c.2077+397_2077+398insCCACC	XP_016861224.1:n.2077+397_2077+398insCCACC
XR_427361.3:n.2293+397_2293+398insCCACC
NM_000096.4:c.2077+397_2077+398insCCACC MANE Select	NP_000087.2:n.2077+397_2077+398insCCACC
NR_046371.2:n.1902-677_1902-676insCCACC