Canonical Allele Identifier: CA436207719

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148930404T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149212617T>G , CM000665.2:g.149212617T>G	GRCh38
NC_000003.11:g.148930404T>G , CM000665.1:g.148930404T>G	GRCh37
NC_000003.10:g.150413094T>G	NCBI36
NG_011800.1:g.14429A>C
NG_011800.2:g.14429A>C
NG_011800.3:g.14429A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.228A>C MANE Select	ENSP00000264613.6:p.Thr76=
ENST00000264613.10:c.228A>C	ENSP00000264613.6:p.Thr76=
ENST00000455472.3:c.348A>C	ENSP00000426888.1:p.Thr116=
ENST00000481169.5:c.228A>C	ENSP00000418773.1:p.Thr76=
ENST00000490639.5:n.260A>C
NM_000096.3:c.228A>C	NP_000087.1:p.Thr76=
NR_046371.1:n.481A>C
XM_006713499.2:c.228A>C	XP_006713562.1:p.Thr76=
XM_006713500.2:c.228A>C	XP_006713563.1:p.Thr76=
XM_006713501.2:c.228A>C	XP_006713564.1:p.Thr76=
XM_006713502.2:c.228A>C	XP_006713565.1:p.Thr76=
XM_011512435.1:c.228A>C	XP_011510737.1:p.Thr76=
XR_427361.2:n.486A>C
XM_006713499.3:c.228A>C	XP_006713562.1:p.Thr76=
XM_006713500.4:c.228A>C	XP_006713563.1:p.Thr76=
XM_006713501.3:c.228A>C	XP_006713564.1:p.Thr76=
XM_011512435.2:c.228A>C	XP_011510737.1:p.Thr76=
XM_017005734.2:c.228A>C	XP_016861223.1:p.Thr76=
XM_017005735.2:c.228A>C	XP_016861224.1:p.Thr76=
XR_427361.3:n.444A>C
NM_000096.4:c.228A>C MANE Select	NP_000087.2:p.Thr76=
NR_046371.2:n.265A>C