Canonical Allele Identifier: CA2661367

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149212657A>G , CM000665.2:g.149212657A>G	GRCh38
NC_000003.11:g.148930444A>G , CM000665.1:g.148930444A>G	GRCh37
NC_000003.10:g.150413134A>G	NCBI36
NG_011800.1:g.14389T>C
NG_011800.2:g.14389T>C
NG_011800.3:g.14389T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000096.4:c.188T>C MANE Select	NP_000087.2:p.Ile63Thr
ENST00000264613.11:c.188T>C MANE Select	ENSP00000264613.6:p.Ile63Thr
NM_000096.3:c.188T>C	NP_000087.1:p.Ile63Thr
NR_046371.1:n.441T>C
NR_046371.2:n.225T>C
ENST00000264613.10:c.188T>C	ENSP00000264613.6:p.Ile63Thr
ENST00000455472.3:c.308T>C	ENSP00000426888.1:p.Ile103Thr
ENST00000481169.5:c.188T>C	ENSP00000418773.1:p.Ile63Thr
ENST00000490639.5:n.220T>C
XM_006713499.2:c.188T>C	XP_006713562.1:p.Ile63Thr
XM_006713499.3:c.188T>C	XP_006713562.1:p.Ile63Thr
XM_006713500.2:c.188T>C	XP_006713563.1:p.Ile63Thr
XM_006713500.4:c.188T>C	XP_006713563.1:p.Ile63Thr
XM_006713501.2:c.188T>C	XP_006713564.1:p.Ile63Thr
XM_006713501.3:c.188T>C	XP_006713564.1:p.Ile63Thr
XM_006713502.2:c.188T>C	XP_006713565.1:p.Ile63Thr
XM_011512435.1:c.188T>C	XP_011510737.1:p.Ile63Thr
XM_011512435.2:c.188T>C	XP_011510737.1:p.Ile63Thr
XM_017005734.2:c.188T>C	XP_016861223.1:p.Ile63Thr
XM_017005735.2:c.188T>C	XP_016861224.1:p.Ile63Thr
XR_427361.2:n.446T>C
XR_427361.3:n.404T>C