Canonical Allele Identifier: CA354929143

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148895652A>T (hg19) ; chr3:g.149177865A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177865A>T , CM000665.2:g.149177865A>T	GRCh38
NC_000003.11:g.148895652A>T , CM000665.1:g.148895652A>T	GRCh37
NC_000003.10:g.150378342A>T	NCBI36
NG_011800.1:g.49181T>A
NG_011800.2:g.49181T>A
NG_011800.3:g.49181T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2993T>A MANE Select	ENSP00000264613.6:p.Phe998Tyr
ENST00000264613.10:c.2993T>A	ENSP00000264613.6:p.Phe998Tyr
ENST00000460674.5:n.910T>A
ENST00000463556.5:n.515T>A
ENST00000473296.1:n.43T>A
ENST00000479771.5:c.398T>A	ENSP00000420367.1:p.Phe133Tyr
ENST00000481169.5:c.2780T>A	ENSP00000418773.1:p.Phe927Tyr
ENST00000490639.5:n.3025T>A
ENST00000494544.1:c.2342T>A	ENSP00000420545.1:p.Phe781Tyr
NM_000096.3:c.2993T>A	NP_000087.1:p.Phe998Tyr
NR_046371.1:n.3033T>A
XM_006713499.2:c.2993T>A	XP_006713562.1:p.Phe998Tyr
XM_006713500.2:c.2993T>A	XP_006713563.1:p.Phe998Tyr
XM_006713501.2:c.2993T>A	XP_006713564.1:p.Phe998Tyr
XM_011512435.1:c.2993T>A	XP_011510737.1:p.Phe998Tyr
XR_427361.2:n.3251T>A
XM_006713499.3:c.2993T>A	XP_006713562.1:p.Phe998Tyr
XM_006713500.4:c.2993T>A	XP_006713563.1:p.Phe998Tyr
XM_006713501.3:c.2993T>A	XP_006713564.1:p.Phe998Tyr
XM_011512435.2:c.2993T>A	XP_011510737.1:p.Phe998Tyr
XM_017005734.2:c.2993T>A	XP_016861223.1:p.Phe998Tyr
XM_017005735.2:c.2993T>A	XP_016861224.1:p.Phe998Tyr
XR_427361.3:n.3209T>A
NM_000096.4:c.2993T>A MANE Select	NP_000087.2:p.Phe998Tyr
NR_046371.2:n.2817T>A