Canonical Allele Identifier: CA354932518

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148904426G>T (hg19) ; chr3:g.149186639G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186639G>T , CM000665.2:g.149186639G>T	GRCh38
NC_000003.11:g.148904426G>T , CM000665.1:g.148904426G>T	GRCh37
NC_000003.10:g.150387116G>T	NCBI36
NG_011800.1:g.40407C>A
NG_011800.2:g.40407C>A
NG_011800.3:g.40407C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.1958C>A MANE Select	ENSP00000264613.6:p.Ala653Asp
ENST00000264613.10:c.1958C>A	ENSP00000264613.6:p.Ala653Asp
ENST00000462336.5:n.332C>A
ENST00000481169.5:c.1865-1193C>A	ENSP00000418773.1:n.1865-1193C>A
ENST00000489736.5:n.1183C>A
ENST00000490639.5:n.1990C>A
ENST00000494544.1:c.1307C>A	ENSP00000420545.1:p.Ala436Asp
ENST00000497902.5:n.139C>A
NM_000096.3:c.1958C>A	NP_000087.1:p.Ala653Asp
NR_046371.1:n.2118-1193C>A
XM_006713499.2:c.1958C>A	XP_006713562.1:p.Ala653Asp
XM_006713500.2:c.1958C>A	XP_006713563.1:p.Ala653Asp
XM_006713501.2:c.1958C>A	XP_006713564.1:p.Ala653Asp
XM_006713502.2:c.1958C>A	XP_006713565.1:p.Ala653Asp
XM_011512435.1:c.1958C>A	XP_011510737.1:p.Ala653Asp
XR_427361.2:n.2216C>A
XM_006713499.3:c.1958C>A	XP_006713562.1:p.Ala653Asp
XM_006713500.4:c.1958C>A	XP_006713563.1:p.Ala653Asp
XM_006713501.3:c.1958C>A	XP_006713564.1:p.Ala653Asp
XM_011512435.2:c.1958C>A	XP_011510737.1:p.Ala653Asp
XM_017005734.2:c.1958C>A	XP_016861223.1:p.Ala653Asp
XM_017005735.2:c.1958C>A	XP_016861224.1:p.Ala653Asp
XR_427361.3:n.2174C>A
NM_000096.4:c.1958C>A MANE Select	NP_000087.2:p.Ala653Asp
NR_046371.2:n.1902-1193C>A