Canonical Allele Identifier: CA344649

Gene: CP

Linked Data

• ClinVar Variation Id: 42172
• ClinVar RCV Id: RCV000035000
• dbSNP Id: rs386134136
• gnomAD v4: 3-149210166-C-T
• COSMIC: COSM3915107
• MyVariant Identifiers: chr3:g.148927953C>T (hg19) ; chr3:g.149210166C>T (hg38)
• PubMed: PMID:20301666

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149210166C>T , CM000665.2:g.149210166C>T	GRCh38
NC_000003.11:g.148927953C>T , CM000665.1:g.148927953C>T	GRCh37
NC_000003.10:g.150410643C>T	NCBI36
NG_011800.1:g.16880G>A
NG_011800.2:g.16880G>A
NG_011800.3:g.16880G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.607+1G>A MANE Select	ENSP00000264613.6:n.607+1G>A
ENST00000264613.10:c.607+1G>A	ENSP00000264613.6:n.607+1G>A
ENST00000481169.5:c.607+1G>A	ENSP00000418773.1:n.607+1G>A
ENST00000490639.5:n.639+1G>A
NM_000096.3:c.607+1G>A	NP_000087.1:n.607+1G>A
NR_046371.1:n.860+1G>A
XM_006713499.2:c.607+1G>A	XP_006713562.1:n.607+1G>A
XM_006713500.2:c.607+1G>A	XP_006713563.1:n.607+1G>A
XM_006713501.2:c.607+1G>A	XP_006713564.1:n.607+1G>A
XM_006713502.2:c.607+1G>A	XP_006713565.1:n.607+1G>A
XM_011512435.1:c.607+1G>A	XP_011510737.1:n.607+1G>A
XR_427361.2:n.865+1G>A
XM_006713499.3:c.607+1G>A	XP_006713562.1:n.607+1G>A
XM_006713500.4:c.607+1G>A	XP_006713563.1:n.607+1G>A
XM_006713501.3:c.607+1G>A	XP_006713564.1:n.607+1G>A
XM_011512435.2:c.607+1G>A	XP_011510737.1:n.607+1G>A
XM_017005734.2:c.607+1G>A	XP_016861223.1:n.607+1G>A
XM_017005735.2:c.607+1G>A	XP_016861224.1:n.607+1G>A
XR_427361.3:n.823+1G>A
NM_000096.4:c.607+1G>A MANE Select	NP_000087.2:n.607+1G>A
NR_046371.2:n.644+1G>A