Canonical Allele Identifier: CA354929144

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148895653A>T (hg19) ; chr3:g.149177866A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177866A>T , CM000665.2:g.149177866A>T	GRCh38
NC_000003.11:g.148895653A>T , CM000665.1:g.148895653A>T	GRCh37
NC_000003.10:g.150378343A>T	NCBI36
NG_011800.1:g.49180T>A
NG_011800.2:g.49180T>A
NG_011800.3:g.49180T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2992T>A MANE Select	ENSP00000264613.6:p.Phe998Ile
ENST00000264613.10:c.2992T>A	ENSP00000264613.6:p.Phe998Ile
ENST00000460674.5:n.909T>A
ENST00000463556.5:n.514T>A
ENST00000473296.1:n.42T>A
ENST00000479771.5:c.397T>A	ENSP00000420367.1:p.Phe133Ile
ENST00000481169.5:c.2779T>A	ENSP00000418773.1:p.Phe927Ile
ENST00000490639.5:n.3024T>A
ENST00000494544.1:c.2341T>A	ENSP00000420545.1:p.Phe781Ile
NM_000096.3:c.2992T>A	NP_000087.1:p.Phe998Ile
NR_046371.1:n.3032T>A
XM_006713499.2:c.2992T>A	XP_006713562.1:p.Phe998Ile
XM_006713500.2:c.2992T>A	XP_006713563.1:p.Phe998Ile
XM_006713501.2:c.2992T>A	XP_006713564.1:p.Phe998Ile
XM_011512435.1:c.2992T>A	XP_011510737.1:p.Phe998Ile
XR_427361.2:n.3250T>A
XM_006713499.3:c.2992T>A	XP_006713562.1:p.Phe998Ile
XM_006713500.4:c.2992T>A	XP_006713563.1:p.Phe998Ile
XM_006713501.3:c.2992T>A	XP_006713564.1:p.Phe998Ile
XM_011512435.2:c.2992T>A	XP_011510737.1:p.Phe998Ile
XM_017005734.2:c.2992T>A	XP_016861223.1:p.Phe998Ile
XM_017005735.2:c.2992T>A	XP_016861224.1:p.Phe998Ile
XR_427361.3:n.3208T>A
NM_000096.4:c.2992T>A MANE Select	NP_000087.2:p.Phe998Ile
NR_046371.2:n.2816T>A