Canonical Allele Identifier: CA1410108148

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177867A= , CM000665.2:g.149177867A=	GRCh38
NC_000003.11:g.148895654A= , CM000665.1:g.148895654A=	GRCh37
NC_000003.10:g.150378344A=	NCBI36
NG_011800.1:g.49179T=
NG_011800.2:g.49179T=
NG_011800.3:g.49179T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2991T= MANE Select	ENSP00000264613.6:p.His997=
ENST00000264613.10:c.2991T=	ENSP00000264613.6:p.His997=
ENST00000460674.5:n.908T=
ENST00000463556.5:n.513T=
ENST00000473296.1:n.41T=
ENST00000479771.5:c.396T=	ENSP00000420367.1:p.His132=
ENST00000481169.5:c.2778T=	ENSP00000418773.1:p.His926=
ENST00000490639.5:n.3023T=
ENST00000494544.1:c.2340T=	ENSP00000420545.1:p.His780=
NM_000096.3:c.2991T=	NP_000087.1:p.His997=
NR_046371.1:n.3031T=
XM_006713499.2:c.2991T=	XP_006713562.1:p.His997=
XM_006713500.2:c.2991T=	XP_006713563.1:p.His997=
XM_006713501.2:c.2991T=	XP_006713564.1:p.His997=
XM_011512435.1:c.2991T=	XP_011510737.1:p.His997=
XR_427361.2:n.3249T=
XM_006713499.3:c.2991T=	XP_006713562.1:p.His997=
XM_006713500.4:c.2991T=	XP_006713563.1:p.His997=
XM_006713501.3:c.2991T=	XP_006713564.1:p.His997=
XM_011512435.2:c.2991T=	XP_011510737.1:p.His997=
XM_017005734.2:c.2991T=	XP_016861223.1:p.His997=
XM_017005735.2:c.2991T=	XP_016861224.1:p.His997=
XR_427361.3:n.3207T=
NM_000096.4:c.2991T= MANE Select	NP_000087.2:p.His997=
NR_046371.2:n.2815T=