Canonical Allele Identifier: CA1410105660

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149187044_149187047delinsATAT , CM000665.2:g.149187044_149187047delinsATAT	GRCh38
NC_000003.11:g.148904831_148904834delinsATAT , CM000665.1:g.148904831_148904834delinsATAT	GRCh37
NC_000003.10:g.150387521_150387524delinsATAT	NCBI36
NG_011800.1:g.39999_40002delinsATAT
NG_011800.2:g.39999_40002delinsATAT
NG_011800.3:g.39999_40002delinsATAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.1865-315_1865-312delinsATAT MANE Select	ENSP00000264613.6:n.1865-315_1865-312delinsATAT
ENST00000264613.10:c.1865-315_1865-312delinsATAT	ENSP00000264613.6:n.1865-315_1865-312delinsATAT
ENST00000462336.5:n.239-315_239-312delinsATAT
ENST00000481169.5:c.1864+1005_1864+1008delinsATAT	ENSP00000418773.1:n.1864+1005_1864+1008delinsATAT
ENST00000489736.5:n.1090-315_1090-312delinsATAT
ENST00000490639.5:n.1897-315_1897-312delinsATAT
ENST00000494544.1:c.1214-315_1214-312delinsATAT	ENSP00000420545.1:n.1214-315_1214-312delinsATAT
ENST00000497902.5:n.46-315_46-312delinsATAT
NM_000096.3:c.1865-315_1865-312delinsATAT	NP_000087.1:n.1865-315_1865-312delinsATAT
NR_046371.1:n.2117+1005_2117+1008delinsATAT
XM_006713499.2:c.1865-315_1865-312delinsATAT	XP_006713562.1:n.1865-315_1865-312delinsATAT
XM_006713500.2:c.1865-315_1865-312delinsATAT	XP_006713563.1:n.1865-315_1865-312delinsATAT
XM_006713501.2:c.1865-315_1865-312delinsATAT	XP_006713564.1:n.1865-315_1865-312delinsATAT
XM_006713502.2:c.1865-315_1865-312delinsATAT	XP_006713565.1:n.1865-315_1865-312delinsATAT
XM_011512435.1:c.1865-315_1865-312delinsATAT	XP_011510737.1:n.1865-315_1865-312delinsATAT
XR_427361.2:n.2123-315_2123-312delinsATAT
XM_006713499.3:c.1865-315_1865-312delinsATAT	XP_006713562.1:n.1865-315_1865-312delinsATAT
XM_006713500.4:c.1865-315_1865-312delinsATAT	XP_006713563.1:n.1865-315_1865-312delinsATAT
XM_006713501.3:c.1865-315_1865-312delinsATAT	XP_006713564.1:n.1865-315_1865-312delinsATAT
XM_011512435.2:c.1865-315_1865-312delinsATAT	XP_011510737.1:n.1865-315_1865-312delinsATAT
XM_017005734.2:c.1865-315_1865-312delinsATAT	XP_016861223.1:n.1865-315_1865-312delinsATAT
XM_017005735.2:c.1865-315_1865-312delinsATAT	XP_016861224.1:n.1865-315_1865-312delinsATAT
XR_427361.3:n.2081-315_2081-312delinsATAT
NM_000096.4:c.1865-315_1865-312delinsATAT MANE Select	NP_000087.2:n.1865-315_1865-312delinsATAT
NR_046371.2:n.1901+1005_1901+1008delinsATAT