Canonical Allele Identifier: CA436205258

Gene: CP

Linked Data

• dbSNP Id: rs1442290146
• gnomAD v2: 3-148916202-C-T
• gnomAD v4: 3-149198415-C-T
• MyVariant Identifiers: chr3:g.148916202C>T (hg19) ; chr3:g.149198415C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149198415C>T , CM000665.2:g.149198415C>T	GRCh38
NC_000003.11:g.148916202C>T , CM000665.1:g.148916202C>T	GRCh37
NC_000003.10:g.150398892C>T	NCBI36
NG_011800.1:g.28631G>A
NG_011800.2:g.28631G>A
NG_011800.3:g.28631G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.1665G>A MANE Select	ENSP00000264613.6:p.Gly555=
ENST00000264613.10:c.1665G>A	ENSP00000264613.6:p.Gly555=
ENST00000462336.5:n.39G>A
ENST00000471356.1:n.484G>A
ENST00000481169.5:c.1665G>A	ENSP00000418773.1:p.Gly555=
ENST00000489736.5:n.890G>A
ENST00000490639.5:n.1697G>A
ENST00000494544.1:c.1014G>A	ENSP00000420545.1:p.Gly338=
ENST00000497797.5:n.274G>A
NM_000096.3:c.1665G>A	NP_000087.1:p.Gly555=
NR_046371.1:n.1918G>A
XM_006713499.2:c.1665G>A	XP_006713562.1:p.Gly555=
XM_006713500.2:c.1665G>A	XP_006713563.1:p.Gly555=
XM_006713501.2:c.1665G>A	XP_006713564.1:p.Gly555=
XM_006713502.2:c.1665G>A	XP_006713565.1:p.Gly555=
XM_011512435.1:c.1665G>A	XP_011510737.1:p.Gly555=
XR_427361.2:n.1923G>A
XM_006713499.3:c.1665G>A	XP_006713562.1:p.Gly555=
XM_006713500.4:c.1665G>A	XP_006713563.1:p.Gly555=
XM_006713501.3:c.1665G>A	XP_006713564.1:p.Gly555=
XM_011512435.2:c.1665G>A	XP_011510737.1:p.Gly555=
XM_017005734.2:c.1665G>A	XP_016861223.1:p.Gly555=
XM_017005735.2:c.1665G>A	XP_016861224.1:p.Gly555=
XR_427361.3:n.1881G>A
NM_000096.4:c.1665G>A MANE Select	NP_000087.2:p.Gly555=
NR_046371.2:n.1702G>A