Canonical Allele Identifier: CA436205254

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148916199T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149198412T>C , CM000665.2:g.149198412T>C	GRCh38
NC_000003.11:g.148916199T>C , CM000665.1:g.148916199T>C	GRCh37
NC_000003.10:g.150398889T>C	NCBI36
NG_011800.1:g.28634A>G
NG_011800.2:g.28634A>G
NG_011800.3:g.28634A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.1668A>G MANE Select	ENSP00000264613.6:p.Pro556=
ENST00000264613.10:c.1668A>G	ENSP00000264613.6:p.Pro556=
ENST00000462336.5:n.42A>G
ENST00000471356.1:n.487A>G
ENST00000481169.5:c.1668A>G	ENSP00000418773.1:p.Pro556=
ENST00000489736.5:n.893A>G
ENST00000490639.5:n.1700A>G
ENST00000494544.1:c.1017A>G	ENSP00000420545.1:p.Pro339=
ENST00000497797.5:n.277A>G
NM_000096.3:c.1668A>G	NP_000087.1:p.Pro556=
NR_046371.1:n.1921A>G
XM_006713499.2:c.1668A>G	XP_006713562.1:p.Pro556=
XM_006713500.2:c.1668A>G	XP_006713563.1:p.Pro556=
XM_006713501.2:c.1668A>G	XP_006713564.1:p.Pro556=
XM_006713502.2:c.1668A>G	XP_006713565.1:p.Pro556=
XM_011512435.1:c.1668A>G	XP_011510737.1:p.Pro556=
XR_427361.2:n.1926A>G
XM_006713499.3:c.1668A>G	XP_006713562.1:p.Pro556=
XM_006713500.4:c.1668A>G	XP_006713563.1:p.Pro556=
XM_006713501.3:c.1668A>G	XP_006713564.1:p.Pro556=
XM_011512435.2:c.1668A>G	XP_011510737.1:p.Pro556=
XM_017005734.2:c.1668A>G	XP_016861223.1:p.Pro556=
XM_017005735.2:c.1668A>G	XP_016861224.1:p.Pro556=
XR_427361.3:n.1884A>G
NM_000096.4:c.1668A>G MANE Select	NP_000087.2:p.Pro556=
NR_046371.2:n.1705A>G