Canonical Allele Identifier: CA1410122623
Gene: CP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149212619T= , CM000665.2:g.149212619T= GRCh38
NC_000003.11:g.148930406T= , CM000665.1:g.148930406T= GRCh37
NC_000003.10:g.150413096T= NCBI36
NG_011800.1:g.14427A=
NG_011800.2:g.14427A=
NG_011800.3:g.14427A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264613.11:c.226A= MANE Select ENSP00000264613.6:p.Thr76=
ENST00000264613.10:c.226A= ENSP00000264613.6:p.Thr76=
ENST00000455472.3:c.346A= ENSP00000426888.1:p.Thr116=
ENST00000481169.5:c.226A= ENSP00000418773.1:p.Thr76=
ENST00000490639.5:n.258A=
NM_000096.3:c.226A= NP_000087.1:p.Thr76=
NR_046371.1:n.479A=
XM_006713499.2:c.226A= XP_006713562.1:p.Thr76=
XM_006713500.2:c.226A= XP_006713563.1:p.Thr76=
XM_006713501.2:c.226A= XP_006713564.1:p.Thr76=
XM_006713502.2:c.226A= XP_006713565.1:p.Thr76=
XM_011512435.1:c.226A= XP_011510737.1:p.Thr76=
XR_427361.2:n.484A=
XM_006713499.3:c.226A= XP_006713562.1:p.Thr76=
XM_006713500.4:c.226A= XP_006713563.1:p.Thr76=
XM_006713501.3:c.226A= XP_006713564.1:p.Thr76=
XM_011512435.2:c.226A= XP_011510737.1:p.Thr76=
XM_017005734.2:c.226A= XP_016861223.1:p.Thr76=
XM_017005735.2:c.226A= XP_016861224.1:p.Thr76=
XR_427361.3:n.442A=
NM_000096.4:c.226A= MANE Select NP_000087.2:p.Thr76=
NR_046371.2:n.263A=