Canonical Allele Identifier: CA1410105165

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186521C= , CM000665.2:g.149186521C=	GRCh38
NC_000003.11:g.148904308C= , CM000665.1:g.148904308C=	GRCh37
NC_000003.10:g.150386998C=	NCBI36
NG_011800.1:g.40525G=
NG_011800.2:g.40525G=
NG_011800.3:g.40525G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2076G= MANE Select	ENSP00000264613.6:p.Glu692=
ENST00000264613.10:c.2076G=	ENSP00000264613.6:p.Glu692=
ENST00000462336.5:n.450G=
ENST00000481169.5:c.1865-1075G=	ENSP00000418773.1:n.1865-1075G=
ENST00000489736.5:n.1301G=
ENST00000490639.5:n.2108G=
ENST00000494544.1:c.1425G=	ENSP00000420545.1:p.Glu475=
ENST00000497902.5:n.257G=
NM_000096.3:c.2076G=	NP_000087.1:p.Glu692=
NR_046371.1:n.2118-1075G=
XM_006713499.2:c.2076G=	XP_006713562.1:p.Glu692=
XM_006713500.2:c.2076G=	XP_006713563.1:p.Glu692=
XM_006713501.2:c.2076G=	XP_006713564.1:p.Glu692=
XM_006713502.2:c.2076G=	XP_006713565.1:p.Glu692=
XM_011512435.1:c.2076G=	XP_011510737.1:p.Glu692=
XR_427361.2:n.2334G=
XM_006713499.3:c.2076G=	XP_006713562.1:p.Glu692=
XM_006713500.4:c.2076G=	XP_006713563.1:p.Glu692=
XM_006713501.3:c.2076G=	XP_006713564.1:p.Glu692=
XM_011512435.2:c.2076G=	XP_011510737.1:p.Glu692=
XM_017005734.2:c.2076G=	XP_016861223.1:p.Glu692=
XM_017005735.2:c.2076G=	XP_016861224.1:p.Glu692=
XR_427361.3:n.2292G=
NM_000096.4:c.2076G= MANE Select	NP_000087.2:p.Glu692=
NR_046371.2:n.1902-1075G=