Canonical Allele Identifier: CA1410105350
Gene: CP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149186633A= , CM000665.2:g.149186633A= GRCh38
NC_000003.11:g.148904420A= , CM000665.1:g.148904420A= GRCh37
NC_000003.10:g.150387110A= NCBI36
NG_011800.1:g.40413T=
NG_011800.2:g.40413T=
NG_011800.3:g.40413T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264613.11:c.1964T= MANE Select ENSP00000264613.6:p.Val655=
ENST00000264613.10:c.1964T= ENSP00000264613.6:p.Val655=
ENST00000462336.5:n.338T=
ENST00000481169.5:c.1865-1187T= ENSP00000418773.1:n.1865-1187T=
ENST00000489736.5:n.1189T=
ENST00000490639.5:n.1996T=
ENST00000494544.1:c.1313T= ENSP00000420545.1:p.Val438=
ENST00000497902.5:n.145T=
NM_000096.3:c.1964T= NP_000087.1:p.Val655=
NR_046371.1:n.2118-1187T=
XM_006713499.2:c.1964T= XP_006713562.1:p.Val655=
XM_006713500.2:c.1964T= XP_006713563.1:p.Val655=
XM_006713501.2:c.1964T= XP_006713564.1:p.Val655=
XM_006713502.2:c.1964T= XP_006713565.1:p.Val655=
XM_011512435.1:c.1964T= XP_011510737.1:p.Val655=
XR_427361.2:n.2222T=
XM_006713499.3:c.1964T= XP_006713562.1:p.Val655=
XM_006713500.4:c.1964T= XP_006713563.1:p.Val655=
XM_006713501.3:c.1964T= XP_006713564.1:p.Val655=
XM_011512435.2:c.1964T= XP_011510737.1:p.Val655=
XM_017005734.2:c.1964T= XP_016861223.1:p.Val655=
XM_017005735.2:c.1964T= XP_016861224.1:p.Val655=
XR_427361.3:n.2180T=
NM_000096.4:c.1964T= MANE Select NP_000087.2:p.Val655=
NR_046371.2:n.1902-1187T=