Canonical Allele Identifier: CA1410108157

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177882G= , CM000665.2:g.149177882G=	GRCh38
NC_000003.11:g.148895669G= , CM000665.1:g.148895669G=	GRCh37
NC_000003.10:g.150378359G=	NCBI36
NG_011800.1:g.49164C=
NG_011800.2:g.49164C=
NG_011800.3:g.49164C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2976C= MANE Select	ENSP00000264613.6:p.Asp992=
ENST00000264613.10:c.2976C=	ENSP00000264613.6:p.Asp992=
ENST00000460674.5:n.893C=
ENST00000463556.5:n.498C=
ENST00000473296.1:n.26C=
ENST00000479771.5:c.381C=	ENSP00000420367.1:p.Asp127=
ENST00000481169.5:c.2763C=	ENSP00000418773.1:p.Asp921=
ENST00000490639.5:n.3008C=
ENST00000494544.1:c.2325C=	ENSP00000420545.1:p.Asp775=
NM_000096.3:c.2976C=	NP_000087.1:p.Asp992=
NR_046371.1:n.3016C=
XM_006713499.2:c.2976C=	XP_006713562.1:p.Asp992=
XM_006713500.2:c.2976C=	XP_006713563.1:p.Asp992=
XM_006713501.2:c.2976C=	XP_006713564.1:p.Asp992=
XM_011512435.1:c.2976C=	XP_011510737.1:p.Asp992=
XR_427361.2:n.3234C=
XM_006713499.3:c.2976C=	XP_006713562.1:p.Asp992=
XM_006713500.4:c.2976C=	XP_006713563.1:p.Asp992=
XM_006713501.3:c.2976C=	XP_006713564.1:p.Asp992=
XM_011512435.2:c.2976C=	XP_011510737.1:p.Asp992=
XM_017005734.2:c.2976C=	XP_016861223.1:p.Asp992=
XM_017005735.2:c.2976C=	XP_016861224.1:p.Asp992=
XR_427361.3:n.3192C=
NM_000096.4:c.2976C= MANE Select	NP_000087.2:p.Asp992=
NR_046371.2:n.2800C=