Canonical Allele Identifier: CA1410111645

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186107A= , CM000665.2:g.149186107A=	GRCh38
NC_000003.11:g.148903894A= , CM000665.1:g.148903894A=	GRCh37
NC_000003.10:g.150386584A=	NCBI36
NG_011800.1:g.40939T=
NG_011800.2:g.40939T=
NG_011800.3:g.40939T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2077+413T= MANE Select	ENSP00000264613.6:n.2077+413T=
ENST00000264613.10:c.2077+413T=	ENSP00000264613.6:n.2077+413T=
ENST00000462336.5:n.451+413T=
ENST00000481169.5:c.1865-661T=	ENSP00000418773.1:n.1865-661T=
ENST00000489736.5:n.1715T=
ENST00000490639.5:n.2109+413T=
ENST00000494544.1:c.1426+413T=	ENSP00000420545.1:n.1426+413T=
ENST00000497902.5:n.258+413T=
NM_000096.3:c.2077+413T=	NP_000087.1:n.2077+413T=
NR_046371.1:n.2118-661T=
XM_006713499.2:c.2077+413T=	XP_006713562.1:n.2077+413T=
XM_006713500.2:c.2077+413T=	XP_006713563.1:n.2077+413T=
XM_006713501.2:c.2077+413T=	XP_006713564.1:n.2077+413T=
XM_006713502.2:c.2077+413T=	XP_006713565.1:n.2077+413T=
XM_011512435.1:c.2077+413T=	XP_011510737.1:n.2077+413T=
XR_427361.2:n.2335+413T=
XM_006713499.3:c.2077+413T=	XP_006713562.1:n.2077+413T=
XM_006713500.4:c.2077+413T=	XP_006713563.1:n.2077+413T=
XM_006713501.3:c.2077+413T=	XP_006713564.1:n.2077+413T=
XM_011512435.2:c.2077+413T=	XP_011510737.1:n.2077+413T=
XM_017005734.2:c.2077+413T=	XP_016861223.1:n.2077+413T=
XM_017005735.2:c.2077+413T=	XP_016861224.1:n.2077+413T=
XR_427361.3:n.2293+413T=
NM_000096.4:c.2077+413T= MANE Select	NP_000087.2:n.2077+413T=
NR_046371.2:n.1902-661T=