Canonical Allele Identifier: CA1410111618

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186040_149186041delinsTG , CM000665.2:g.149186040_149186041delinsTG	GRCh38
NC_000003.11:g.148903827_148903828delinsTG , CM000665.1:g.148903827_148903828delinsTG	GRCh37
NC_000003.10:g.150386517_150386518delinsTG	NCBI36
NG_011800.1:g.41005_41006delinsCA
NG_011800.2:g.41005_41006delinsCA
NG_011800.3:g.41005_41006delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2077+479_2077+480delinsCA MANE Select	ENSP00000264613.6:n.2077+479_2077+480delinsCA
ENST00000264613.10:c.2077+479_2077+480delinsCA	ENSP00000264613.6:n.2077+479_2077+480delinsCA
ENST00000462336.5:n.451+479_451+480delinsCA
ENST00000481169.5:c.1865-595_1865-594delinsCA	ENSP00000418773.1:n.1865-595_1865-594delinsCA
ENST00000490639.5:n.2109+479_2109+480delinsCA
ENST00000494544.1:c.1426+479_1426+480delinsCA	ENSP00000420545.1:n.1426+479_1426+480delinsCA
ENST00000497902.5:n.258+479_258+480delinsCA
NM_000096.3:c.2077+479_2077+480delinsCA	NP_000087.1:n.2077+479_2077+480delinsCA
NR_046371.1:n.2118-595_2118-594delinsCA
XM_006713499.2:c.2077+479_2077+480delinsCA	XP_006713562.1:n.2077+479_2077+480delinsCA
XM_006713500.2:c.2077+479_2077+480delinsCA	XP_006713563.1:n.2077+479_2077+480delinsCA
XM_006713501.2:c.2077+479_2077+480delinsCA	XP_006713564.1:n.2077+479_2077+480delinsCA
XM_006713502.2:c.2077+479_2077+480delinsCA	XP_006713565.1:n.2077+479_2077+480delinsCA
XM_011512435.1:c.2077+479_2077+480delinsCA	XP_011510737.1:n.2077+479_2077+480delinsCA
XR_427361.2:n.2335+479_2335+480delinsCA
XM_006713499.3:c.2077+479_2077+480delinsCA	XP_006713562.1:n.2077+479_2077+480delinsCA
XM_006713500.4:c.2077+479_2077+480delinsCA	XP_006713563.1:n.2077+479_2077+480delinsCA
XM_006713501.3:c.2077+479_2077+480delinsCA	XP_006713564.1:n.2077+479_2077+480delinsCA
XM_011512435.2:c.2077+479_2077+480delinsCA	XP_011510737.1:n.2077+479_2077+480delinsCA
XM_017005734.2:c.2077+479_2077+480delinsCA	XP_016861223.1:n.2077+479_2077+480delinsCA
XM_017005735.2:c.2077+479_2077+480delinsCA	XP_016861224.1:n.2077+479_2077+480delinsCA
XR_427361.3:n.2293+479_2293+480delinsCA
NM_000096.4:c.2077+479_2077+480delinsCA MANE Select	NP_000087.2:n.2077+479_2077+480delinsCA
NR_046371.2:n.1902-595_1902-594delinsCA