Canonical Allele Identifier: CA2668139749

Gene: CP

Linked Data

• gnomAD v4: 3-149186757-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186757T>C , CM000665.2:g.149186757T>C	GRCh38
NC_000003.11:g.148904544T>C , CM000665.1:g.148904544T>C	GRCh37
NC_000003.10:g.150387234T>C	NCBI36
NG_011800.1:g.40289A>G
NG_011800.2:g.40289A>G
NG_011800.3:g.40289A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.1865-25A>G MANE Select	ENSP00000264613.6:n.1865-25A>G
ENST00000264613.10:c.1865-25A>G	ENSP00000264613.6:n.1865-25A>G
ENST00000462336.5:n.239-25A>G
ENST00000481169.5:c.1864+1295A>G	ENSP00000418773.1:n.1864+1295A>G
ENST00000489736.5:n.1090-25A>G
ENST00000490639.5:n.1897-25A>G
ENST00000494544.1:c.1214-25A>G	ENSP00000420545.1:n.1214-25A>G
ENST00000497902.5:n.46-25A>G
NM_000096.3:c.1865-25A>G	NP_000087.1:n.1865-25A>G
NR_046371.1:n.2117+1295A>G
XM_006713499.2:c.1865-25A>G	XP_006713562.1:n.1865-25A>G
XM_006713500.2:c.1865-25A>G	XP_006713563.1:n.1865-25A>G
XM_006713501.2:c.1865-25A>G	XP_006713564.1:n.1865-25A>G
XM_006713502.2:c.1865-25A>G	XP_006713565.1:n.1865-25A>G
XM_011512435.1:c.1865-25A>G	XP_011510737.1:n.1865-25A>G
XR_427361.2:n.2123-25A>G
XM_006713499.3:c.1865-25A>G	XP_006713562.1:n.1865-25A>G
XM_006713500.4:c.1865-25A>G	XP_006713563.1:n.1865-25A>G
XM_006713501.3:c.1865-25A>G	XP_006713564.1:n.1865-25A>G
XM_011512435.2:c.1865-25A>G	XP_011510737.1:n.1865-25A>G
XM_017005734.2:c.1865-25A>G	XP_016861223.1:n.1865-25A>G
XM_017005735.2:c.1865-25A>G	XP_016861224.1:n.1865-25A>G
XR_427361.3:n.2081-25A>G
NM_000096.4:c.1865-25A>G MANE Select	NP_000087.2:n.1865-25A>G
NR_046371.2:n.1901+1295A>G