Canonical Allele Identifier: CA1410108141
Gene: CP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149177855A= , CM000665.2:g.149177855A= GRCh38
NC_000003.11:g.148895642A= , CM000665.1:g.148895642A= GRCh37
NC_000003.10:g.150378332A= NCBI36
NG_011800.1:g.49191T=
NG_011800.2:g.49191T=
NG_011800.3:g.49191T=

Transcript Alleles

HGVS Amino-acid change
ENST00000264613.11:c.3003T= MANE Select ENSP00000264613.6:p.His1001=
ENST00000264613.10:c.3003T= ENSP00000264613.6:p.His1001=
ENST00000460674.5:n.920T=
ENST00000463556.5:n.525T=
ENST00000473296.1:n.53T=
ENST00000479771.5:c.408T= ENSP00000420367.1:p.His136=
ENST00000481169.5:c.2790T= ENSP00000418773.1:p.His930=
ENST00000490639.5:n.3035T=
ENST00000494544.1:c.2352T= ENSP00000420545.1:p.His784=
NM_000096.3:c.3003T= NP_000087.1:p.His1001=
NR_046371.1:n.3043T=
XM_006713499.2:c.3003T= XP_006713562.1:p.His1001=
XM_006713500.2:c.3003T= XP_006713563.1:p.His1001=
XM_006713501.2:c.3003T= XP_006713564.1:p.His1001=
XM_011512435.1:c.3003T= XP_011510737.1:p.His1001=
XR_427361.2:n.3261T=
XM_006713499.3:c.3003T= XP_006713562.1:p.His1001=
XM_006713500.4:c.3003T= XP_006713563.1:p.His1001=
XM_006713501.3:c.3003T= XP_006713564.1:p.His1001=
XM_011512435.2:c.3003T= XP_011510737.1:p.His1001=
XM_017005734.2:c.3003T= XP_016861223.1:p.His1001=
XM_017005735.2:c.3003T= XP_016861224.1:p.His1001=
XR_427361.3:n.3219T=
NM_000096.4:c.3003T= MANE Select NP_000087.2:p.His1001=
NR_046371.2:n.2827T=