Canonical Allele Identifier: CA2704025025

Gene: CP

Linked Data

• dbSNP Id: rs958720578

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186946A>G , CM000665.2:g.149186946A>G	GRCh38
NC_000003.11:g.148904733A>G , CM000665.1:g.148904733A>G	GRCh37
NC_000003.10:g.150387423A>G	NCBI36
NG_011800.1:g.40100T>C
NG_011800.2:g.40100T>C
NG_011800.3:g.40100T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.1865-214T>C MANE Select	ENSP00000264613.6:n.1865-214T>C
ENST00000264613.10:c.1865-214T>C	ENSP00000264613.6:n.1865-214T>C
ENST00000462336.5:n.239-214T>C
ENST00000481169.5:c.1864+1106T>C	ENSP00000418773.1:n.1864+1106T>C
ENST00000489736.5:n.1090-214T>C
ENST00000490639.5:n.1897-214T>C
ENST00000494544.1:c.1214-214T>C	ENSP00000420545.1:n.1214-214T>C
ENST00000497902.5:n.46-214T>C
NM_000096.3:c.1865-214T>C	NP_000087.1:n.1865-214T>C
NR_046371.1:n.2117+1106T>C
XM_006713499.2:c.1865-214T>C	XP_006713562.1:n.1865-214T>C
XM_006713500.2:c.1865-214T>C	XP_006713563.1:n.1865-214T>C
XM_006713501.2:c.1865-214T>C	XP_006713564.1:n.1865-214T>C
XM_006713502.2:c.1865-214T>C	XP_006713565.1:n.1865-214T>C
XM_011512435.1:c.1865-214T>C	XP_011510737.1:n.1865-214T>C
XR_427361.2:n.2123-214T>C
XM_006713499.3:c.1865-214T>C	XP_006713562.1:n.1865-214T>C
XM_006713500.4:c.1865-214T>C	XP_006713563.1:n.1865-214T>C
XM_006713501.3:c.1865-214T>C	XP_006713564.1:n.1865-214T>C
XM_011512435.2:c.1865-214T>C	XP_011510737.1:n.1865-214T>C
XM_017005734.2:c.1865-214T>C	XP_016861223.1:n.1865-214T>C
XM_017005735.2:c.1865-214T>C	XP_016861224.1:n.1865-214T>C
XR_427361.3:n.2081-214T>C
NM_000096.4:c.1865-214T>C MANE Select	NP_000087.2:n.1865-214T>C
NR_046371.2:n.1901+1106T>C