Canonical Allele Identifier: CA1410108136
Gene: CP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149177842T= , CM000665.2:g.149177842T= GRCh38
NC_000003.11:g.148895629T= , CM000665.1:g.148895629T= GRCh37
NC_000003.10:g.150378319T= NCBI36
NG_011800.1:g.49204A=
NG_011800.2:g.49204A=
NG_011800.3:g.49204A=

Transcript Alleles

HGVS Amino-acid change
ENST00000264613.11:c.3016A= MANE Select ENSP00000264613.6:p.Lys1006=
ENST00000264613.10:c.3016A= ENSP00000264613.6:p.Lys1006=
ENST00000460674.5:n.933A=
ENST00000463556.5:n.538A=
ENST00000473296.1:n.66A=
ENST00000479771.5:c.421A= ENSP00000420367.1:p.Lys141=
ENST00000481169.5:c.2803A= ENSP00000418773.1:p.Lys935=
ENST00000490639.5:n.3048A=
ENST00000494544.1:c.2365A= ENSP00000420545.1:p.Lys789=
NM_000096.3:c.3016A= NP_000087.1:p.Lys1006=
NR_046371.1:n.3056A=
XM_006713499.2:c.3016A= XP_006713562.1:p.Lys1006=
XM_006713500.2:c.3016A= XP_006713563.1:p.Lys1006=
XM_006713501.2:c.3016A= XP_006713564.1:p.Lys1006=
XM_011512435.1:c.3016A= XP_011510737.1:p.Lys1006=
XR_427361.2:n.3274A=
XM_006713499.3:c.3016A= XP_006713562.1:p.Lys1006=
XM_006713500.4:c.3016A= XP_006713563.1:p.Lys1006=
XM_006713501.3:c.3016A= XP_006713564.1:p.Lys1006=
XM_011512435.2:c.3016A= XP_011510737.1:p.Lys1006=
XM_017005734.2:c.3016A= XP_016861223.1:p.Lys1006=
XM_017005735.2:c.3016A= XP_016861224.1:p.Lys1006=
XR_427361.3:n.3232A=
NM_000096.4:c.3016A= MANE Select NP_000087.2:p.Lys1006=
NR_046371.2:n.2840A=