Canonical Allele Identifier: CA1410105172

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186524T= , CM000665.2:g.149186524T=	GRCh38
NC_000003.11:g.148904311T= , CM000665.1:g.148904311T=	GRCh37
NC_000003.10:g.150387001T=	NCBI36
NG_011800.1:g.40522A=
NG_011800.2:g.40522A=
NG_011800.3:g.40522A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2073A= MANE Select	ENSP00000264613.6:p.Thr691=
ENST00000264613.10:c.2073A=	ENSP00000264613.6:p.Thr691=
ENST00000462336.5:n.447A=
ENST00000481169.5:c.1865-1078A=	ENSP00000418773.1:n.1865-1078A=
ENST00000489736.5:n.1298A=
ENST00000490639.5:n.2105A=
ENST00000494544.1:c.1422A=	ENSP00000420545.1:p.Thr474=
ENST00000497902.5:n.254A=
NM_000096.3:c.2073A=	NP_000087.1:p.Thr691=
NR_046371.1:n.2118-1078A=
XM_006713499.2:c.2073A=	XP_006713562.1:p.Thr691=
XM_006713500.2:c.2073A=	XP_006713563.1:p.Thr691=
XM_006713501.2:c.2073A=	XP_006713564.1:p.Thr691=
XM_006713502.2:c.2073A=	XP_006713565.1:p.Thr691=
XM_011512435.1:c.2073A=	XP_011510737.1:p.Thr691=
XR_427361.2:n.2331A=
XM_006713499.3:c.2073A=	XP_006713562.1:p.Thr691=
XM_006713500.4:c.2073A=	XP_006713563.1:p.Thr691=
XM_006713501.3:c.2073A=	XP_006713564.1:p.Thr691=
XM_011512435.2:c.2073A=	XP_011510737.1:p.Thr691=
XM_017005734.2:c.2073A=	XP_016861223.1:p.Thr691=
XM_017005735.2:c.2073A=	XP_016861224.1:p.Thr691=
XR_427361.3:n.2289A=
NM_000096.4:c.2073A= MANE Select	NP_000087.2:p.Thr691=
NR_046371.2:n.1902-1078A=