Canonical Allele Identifier: CA436213529

Gene: CP

Linked Data

• dbSNP Id: rs1341919254
• MyVariant Identifiers: chr3:g.148896305C>T (hg19) ; chr3:g.149178518C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149178518C>T , CM000665.2:g.149178518C>T	GRCh38
NC_000003.11:g.148896305C>T , CM000665.1:g.148896305C>T	GRCh37
NC_000003.10:g.150378995C>T	NCBI36
NG_011800.1:g.48528G>A
NG_011800.2:g.48528G>A
NG_011800.3:g.48528G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.2775G>A MANE Select	ENSP00000264613.6:p.Glu925=
ENST00000264613.10:c.2775G>A	ENSP00000264613.6:p.Glu925=
ENST00000460674.5:n.692G>A
ENST00000463556.5:n.297G>A
ENST00000479771.5:c.180G>A	ENSP00000420367.1:p.Glu60=
ENST00000481169.5:c.2562G>A	ENSP00000418773.1:p.Glu854=
ENST00000490639.5:n.2807G>A
ENST00000494544.1:c.2124G>A	ENSP00000420545.1:p.Glu708=
NM_000096.3:c.2775G>A	NP_000087.1:p.Glu925=
NR_046371.1:n.2815G>A
XM_006713499.2:c.2775G>A	XP_006713562.1:p.Glu925=
XM_006713500.2:c.2775G>A	XP_006713563.1:p.Glu925=
XM_006713501.2:c.2775G>A	XP_006713564.1:p.Glu925=
XM_011512435.1:c.2775G>A	XP_011510737.1:p.Glu925=
XR_427361.2:n.3033G>A
XM_006713499.3:c.2775G>A	XP_006713562.1:p.Glu925=
XM_006713500.4:c.2775G>A	XP_006713563.1:p.Glu925=
XM_006713501.3:c.2775G>A	XP_006713564.1:p.Glu925=
XM_011512435.2:c.2775G>A	XP_011510737.1:p.Glu925=
XM_017005734.2:c.2775G>A	XP_016861223.1:p.Glu925=
XM_017005735.2:c.2775G>A	XP_016861224.1:p.Glu925=
XR_427361.3:n.2991G>A
NM_000096.4:c.2775G>A MANE Select	NP_000087.2:p.Glu925=
NR_046371.2:n.2599G>A