Canonical Allele Identifier: CA1410122670
Gene: CP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149212724A= , CM000665.2:g.149212724A= GRCh38
NC_000003.11:g.148930511A= , CM000665.1:g.148930511A= GRCh37
NC_000003.10:g.150413201A= NCBI36
NG_011800.1:g.14322T=
NG_011800.2:g.14322T=
NG_011800.3:g.14322T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264613.11:c.147-26T= MANE Select ENSP00000264613.6:n.147-26T=
ENST00000264613.10:c.147-26T= ENSP00000264613.6:n.147-26T=
ENST00000455472.3:c.267-26T= ENSP00000426888.1:n.267-26T=
ENST00000481169.5:c.147-26T= ENSP00000418773.1:n.147-26T=
ENST00000490639.5:n.179-26T=
NM_000096.3:c.147-26T= NP_000087.1:n.147-26T=
NR_046371.1:n.400-26T=
XM_006713499.2:c.147-26T= XP_006713562.1:n.147-26T=
XM_006713500.2:c.147-26T= XP_006713563.1:n.147-26T=
XM_006713501.2:c.147-26T= XP_006713564.1:n.147-26T=
XM_006713502.2:c.147-26T= XP_006713565.1:n.147-26T=
XM_011512435.1:c.147-26T= XP_011510737.1:n.147-26T=
XR_427361.2:n.405-26T=
XM_006713499.3:c.147-26T= XP_006713562.1:n.147-26T=
XM_006713500.4:c.147-26T= XP_006713563.1:n.147-26T=
XM_006713501.3:c.147-26T= XP_006713564.1:n.147-26T=
XM_011512435.2:c.147-26T= XP_011510737.1:n.147-26T=
XM_017005734.2:c.147-26T= XP_016861223.1:n.147-26T=
XM_017005735.2:c.147-26T= XP_016861224.1:n.147-26T=
XR_427361.3:n.363-26T=
NM_000096.4:c.147-26T= MANE Select NP_000087.2:n.147-26T=
NR_046371.2:n.184-26T=