Canonical Allele Identifier: CA354930994

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148899878A>T (hg19) ; chr3:g.149182091A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149182091A>T , CM000665.2:g.149182091A>T	GRCh38
NC_000003.11:g.148899878A>T , CM000665.1:g.148899878A>T	GRCh37
NC_000003.10:g.150382568A>T	NCBI36
NG_011800.1:g.44955T>A
NG_011800.2:g.44955T>A
NG_011800.3:g.44955T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2468T>A MANE Select	ENSP00000264613.6:p.Ile823Asn
ENST00000264613.10:c.2468T>A	ENSP00000264613.6:p.Ile823Asn
ENST00000481169.5:c.2255T>A	ENSP00000418773.1:p.Ile752Asn
ENST00000490639.5:n.2500T>A
ENST00000494544.1:c.1817T>A	ENSP00000420545.1:p.Ile606Asn
NM_000096.3:c.2468T>A	NP_000087.1:p.Ile823Asn
NR_046371.1:n.2508T>A
XM_006713499.2:c.2468T>A	XP_006713562.1:p.Ile823Asn
XM_006713500.2:c.2468T>A	XP_006713563.1:p.Ile823Asn
XM_006713501.2:c.2468T>A	XP_006713564.1:p.Ile823Asn
XM_006713502.2:c.2468T>A	XP_006713565.1:p.Ile823Asn
XM_011512435.1:c.2468T>A	XP_011510737.1:p.Ile823Asn
XR_427361.2:n.2726T>A
XM_006713499.3:c.2468T>A	XP_006713562.1:p.Ile823Asn
XM_006713500.4:c.2468T>A	XP_006713563.1:p.Ile823Asn
XM_006713501.3:c.2468T>A	XP_006713564.1:p.Ile823Asn
XM_011512435.2:c.2468T>A	XP_011510737.1:p.Ile823Asn
XM_017005734.2:c.2468T>A	XP_016861223.1:p.Ile823Asn
XM_017005735.2:c.2468T>A	XP_016861224.1:p.Ile823Asn
XR_427361.3:n.2684T>A
NM_000096.4:c.2468T>A MANE Select	NP_000087.2:p.Ile823Asn
NR_046371.2:n.2292T>A