Canonical Allele Identifier: CA85550051

Gene: CP

Linked Data

• dbSNP Id: rs28361508
• MyVariant Identifiers: chr3:g.148930517A>C (hg19) ; chr3:g.149212730A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149212730A>C , CM000665.2:g.149212730A>C	GRCh38
NC_000003.11:g.148930517A>C , CM000665.1:g.148930517A>C	GRCh37
NC_000003.10:g.150413207A>C	NCBI36
NG_011800.1:g.14316T>G
NG_011800.2:g.14316T>G
NG_011800.3:g.14316T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.147-32T>G MANE Select	ENSP00000264613.6:n.147-32T>G
ENST00000264613.10:c.147-32T>G	ENSP00000264613.6:n.147-32T>G
ENST00000455472.3:c.267-32T>G	ENSP00000426888.1:n.267-32T>G
ENST00000481169.5:c.147-32T>G	ENSP00000418773.1:n.147-32T>G
ENST00000490639.5:n.179-32T>G
NM_000096.3:c.147-32T>G	NP_000087.1:n.147-32T>G
NR_046371.1:n.400-32T>G
XM_006713499.2:c.147-32T>G	XP_006713562.1:n.147-32T>G
XM_006713500.2:c.147-32T>G	XP_006713563.1:n.147-32T>G
XM_006713501.2:c.147-32T>G	XP_006713564.1:n.147-32T>G
XM_006713502.2:c.147-32T>G	XP_006713565.1:n.147-32T>G
XM_011512435.1:c.147-32T>G	XP_011510737.1:n.147-32T>G
XR_427361.2:n.405-32T>G
XM_006713499.3:c.147-32T>G	XP_006713562.1:n.147-32T>G
XM_006713500.4:c.147-32T>G	XP_006713563.1:n.147-32T>G
XM_006713501.3:c.147-32T>G	XP_006713564.1:n.147-32T>G
XM_011512435.2:c.147-32T>G	XP_011510737.1:n.147-32T>G
XM_017005734.2:c.147-32T>G	XP_016861223.1:n.147-32T>G
XM_017005735.2:c.147-32T>G	XP_016861224.1:n.147-32T>G
XR_427361.3:n.363-32T>G
NM_000096.4:c.147-32T>G MANE Select	NP_000087.2:n.147-32T>G
NR_046371.2:n.184-32T>G