Canonical Allele Identifier: CA1410105362
Gene: CP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149186639G= , CM000665.2:g.149186639G= GRCh38
NC_000003.11:g.148904426G= , CM000665.1:g.148904426G= GRCh37
NC_000003.10:g.150387116G= NCBI36
NG_011800.1:g.40407C=
NG_011800.2:g.40407C=
NG_011800.3:g.40407C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264613.11:c.1958C= MANE Select ENSP00000264613.6:p.Ala653=
ENST00000264613.10:c.1958C= ENSP00000264613.6:p.Ala653=
ENST00000462336.5:n.332C=
ENST00000481169.5:c.1865-1193C= ENSP00000418773.1:n.1865-1193C=
ENST00000489736.5:n.1183C=
ENST00000490639.5:n.1990C=
ENST00000494544.1:c.1307C= ENSP00000420545.1:p.Ala436=
ENST00000497902.5:n.139C=
NM_000096.3:c.1958C= NP_000087.1:p.Ala653=
NR_046371.1:n.2118-1193C=
XM_006713499.2:c.1958C= XP_006713562.1:p.Ala653=
XM_006713500.2:c.1958C= XP_006713563.1:p.Ala653=
XM_006713501.2:c.1958C= XP_006713564.1:p.Ala653=
XM_006713502.2:c.1958C= XP_006713565.1:p.Ala653=
XM_011512435.1:c.1958C= XP_011510737.1:p.Ala653=
XR_427361.2:n.2216C=
XM_006713499.3:c.1958C= XP_006713562.1:p.Ala653=
XM_006713500.4:c.1958C= XP_006713563.1:p.Ala653=
XM_006713501.3:c.1958C= XP_006713564.1:p.Ala653=
XM_011512435.2:c.1958C= XP_011510737.1:p.Ala653=
XM_017005734.2:c.1958C= XP_016861223.1:p.Ala653=
XM_017005735.2:c.1958C= XP_016861224.1:p.Ala653=
XR_427361.3:n.2174C=
NM_000096.4:c.1958C= MANE Select NP_000087.2:p.Ala653=
NR_046371.2:n.1902-1193C=