Canonical Allele Identifier: CA1410115048

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149195371A= , CM000665.2:g.149195371A=	GRCh38
NC_000003.11:g.148913158A= , CM000665.1:g.148913158A=	GRCh37
NC_000003.10:g.150395848A=	NCBI36
NG_011800.1:g.31675T=
NG_011800.2:g.31675T=
NG_011800.3:g.31675T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.1713+2996T= MANE Select	ENSP00000264613.6:n.1713+2996T=
ENST00000264613.10:c.1713+2996T=	ENSP00000264613.6:n.1713+2996T=
ENST00000462336.5:n.87+2996T=
ENST00000471356.1:n.532+2996T=
ENST00000481169.5:c.1713+2996T=	ENSP00000418773.1:n.1713+2996T=
ENST00000489736.5:n.938+2996T=
ENST00000490639.5:n.1745+2996T=
ENST00000494544.1:c.1062+2996T=	ENSP00000420545.1:n.1062+2996T=
ENST00000497797.5:n.322+2996T=
NM_000096.3:c.1713+2996T=	NP_000087.1:n.1713+2996T=
NR_046371.1:n.1966+2996T=
XM_006713499.2:c.1713+2996T=	XP_006713562.1:n.1713+2996T=
XM_006713500.2:c.1713+2996T=	XP_006713563.1:n.1713+2996T=
XM_006713501.2:c.1713+2996T=	XP_006713564.1:n.1713+2996T=
XM_006713502.2:c.1713+2996T=	XP_006713565.1:n.1713+2996T=
XM_011512435.1:c.1713+2996T=	XP_011510737.1:n.1713+2996T=
XR_427361.2:n.1971+2996T=
XM_006713499.3:c.1713+2996T=	XP_006713562.1:n.1713+2996T=
XM_006713500.4:c.1713+2996T=	XP_006713563.1:n.1713+2996T=
XM_006713501.3:c.1713+2996T=	XP_006713564.1:n.1713+2996T=
XM_011512435.2:c.1713+2996T=	XP_011510737.1:n.1713+2996T=
XM_017005734.2:c.1713+2996T=	XP_016861223.1:n.1713+2996T=
XM_017005735.2:c.1713+2996T=	XP_016861224.1:n.1713+2996T=
XR_427361.3:n.1929+2996T=
NM_000096.4:c.1713+2996T= MANE Select	NP_000087.2:n.1713+2996T=
NR_046371.2:n.1750+2996T=