Canonical Allele Identifier: CA354930943

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148899869T>G (hg19) ; chr3:g.149182082T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149182082T>G , CM000665.2:g.149182082T>G	GRCh38
NC_000003.11:g.148899869T>G , CM000665.1:g.148899869T>G	GRCh37
NC_000003.10:g.150382559T>G	NCBI36
NG_011800.1:g.44964A>C
NG_011800.2:g.44964A>C
NG_011800.3:g.44964A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2477A>C MANE Select	ENSP00000264613.6:p.Asn826Thr
ENST00000264613.10:c.2477A>C	ENSP00000264613.6:p.Asn826Thr
ENST00000481169.5:c.2264A>C	ENSP00000418773.1:p.Asn755Thr
ENST00000490639.5:n.2509A>C
ENST00000494544.1:c.1826A>C	ENSP00000420545.1:p.Asn609Thr
NM_000096.3:c.2477A>C	NP_000087.1:p.Asn826Thr
NR_046371.1:n.2517A>C
XM_006713499.2:c.2477A>C	XP_006713562.1:p.Asn826Thr
XM_006713500.2:c.2477A>C	XP_006713563.1:p.Asn826Thr
XM_006713501.2:c.2477A>C	XP_006713564.1:p.Asn826Thr
XM_006713502.2:c.2477A>C	XP_006713565.1:p.Asn826Thr
XM_011512435.1:c.2477A>C	XP_011510737.1:p.Asn826Thr
XR_427361.2:n.2735A>C
XM_006713499.3:c.2477A>C	XP_006713562.1:p.Asn826Thr
XM_006713500.4:c.2477A>C	XP_006713563.1:p.Asn826Thr
XM_006713501.3:c.2477A>C	XP_006713564.1:p.Asn826Thr
XM_011512435.2:c.2477A>C	XP_011510737.1:p.Asn826Thr
XM_017005734.2:c.2477A>C	XP_016861223.1:p.Asn826Thr
XM_017005735.2:c.2477A>C	XP_016861224.1:p.Asn826Thr
XR_427361.3:n.2693A>C
NM_000096.4:c.2477A>C MANE Select	NP_000087.2:p.Asn826Thr
NR_046371.2:n.2301A>C