Canonical Allele Identifier: CA1410105434

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186675_149186676delinsGA , CM000665.2:g.149186675_149186676delinsGA	GRCh38
NC_000003.11:g.148904462_148904463delinsGA , CM000665.1:g.148904462_148904463delinsGA	GRCh37
NC_000003.10:g.150387152_150387153delinsGA	NCBI36
NG_011800.1:g.40370_40371delinsTC
NG_011800.2:g.40370_40371delinsTC
NG_011800.3:g.40370_40371delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.1921_1922delinsTC MANE Select	ENSP00000264613.6:p.Ser641=
ENST00000264613.10:c.1921_1922delinsTC	ENSP00000264613.6:p.Ser641=
ENST00000462336.5:n.295_296delinsTC
ENST00000481169.5:c.1865-1230_1865-1229delinsTC	ENSP00000418773.1:n.1865-1230_1865-1229delinsTC
ENST00000489736.5:n.1146_1147delinsTC
ENST00000490639.5:n.1953_1954delinsTC
ENST00000494544.1:c.1270_1271delinsTC	ENSP00000420545.1:p.Ser424=
ENST00000497902.5:n.102_103delinsTC
NM_000096.3:c.1921_1922delinsTC	NP_000087.1:p.Ser641=
NR_046371.1:n.2118-1230_2118-1229delinsTC
XM_006713499.2:c.1921_1922delinsTC	XP_006713562.1:p.Ser641=
XM_006713500.2:c.1921_1922delinsTC	XP_006713563.1:p.Ser641=
XM_006713501.2:c.1921_1922delinsTC	XP_006713564.1:p.Ser641=
XM_006713502.2:c.1921_1922delinsTC	XP_006713565.1:p.Ser641=
XM_011512435.1:c.1921_1922delinsTC	XP_011510737.1:p.Ser641=
XR_427361.2:n.2179_2180delinsTC
XM_006713499.3:c.1921_1922delinsTC	XP_006713562.1:p.Ser641=
XM_006713500.4:c.1921_1922delinsTC	XP_006713563.1:p.Ser641=
XM_006713501.3:c.1921_1922delinsTC	XP_006713564.1:p.Ser641=
XM_011512435.2:c.1921_1922delinsTC	XP_011510737.1:p.Ser641=
XM_017005734.2:c.1921_1922delinsTC	XP_016861223.1:p.Ser641=
XM_017005735.2:c.1921_1922delinsTC	XP_016861224.1:p.Ser641=
XR_427361.3:n.2137_2138delinsTC
NM_000096.4:c.1921_1922delinsTC MANE Select	NP_000087.2:p.Ser641=
NR_046371.2:n.1902-1230_1902-1229delinsTC