Canonical Allele Identifier: CA1410108843

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149179510G= , CM000665.2:g.149179510G=	GRCh38
NC_000003.11:g.148897297G= , CM000665.1:g.148897297G=	GRCh37
NC_000003.10:g.150379987G=	NCBI36
NG_011800.1:g.47536C=
NG_011800.2:g.47536C=
NG_011800.3:g.47536C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.2661+46C= MANE Select	ENSP00000264613.6:n.2661+46C=
ENST00000264613.10:c.2661+46C=	ENSP00000264613.6:n.2661+46C=
ENST00000460674.5:n.578+46C=
ENST00000463556.5:n.183+46C=
ENST00000479771.5:c.66+46C=	ENSP00000420367.1:n.66+46C=
ENST00000481169.5:c.2448+46C=	ENSP00000418773.1:n.2448+46C=
ENST00000490639.5:n.2693+46C=
ENST00000494544.1:c.2010+46C=	ENSP00000420545.1:n.2010+46C=
NM_000096.3:c.2661+46C=	NP_000087.1:n.2661+46C=
NR_046371.1:n.2701+46C=
XM_006713499.2:c.2661+46C=	XP_006713562.1:n.2661+46C=
XM_006713500.2:c.2661+46C=	XP_006713563.1:n.2661+46C=
XM_006713501.2:c.2661+46C=	XP_006713564.1:n.2661+46C=
XM_006713502.2:c.2661+46C=	XP_006713565.1:n.2661+46C=
XM_011512435.1:c.2661+46C=	XP_011510737.1:n.2661+46C=
XR_427361.2:n.2919+46C=
XM_006713499.3:c.2661+46C=	XP_006713562.1:n.2661+46C=
XM_006713500.4:c.2661+46C=	XP_006713563.1:n.2661+46C=
XM_006713501.3:c.2661+46C=	XP_006713564.1:n.2661+46C=
XM_011512435.2:c.2661+46C=	XP_011510737.1:n.2661+46C=
XM_017005734.2:c.2661+46C=	XP_016861223.1:n.2661+46C=
XM_017005735.2:c.2661+46C=	XP_016861224.1:n.2661+46C=
XR_427361.3:n.2877+46C=
NM_000096.4:c.2661+46C= MANE Select	NP_000087.2:n.2661+46C=
NR_046371.2:n.2485+46C=