Canonical Allele Identifier: CA354929114

Gene: CP

Linked Data

• MyVariant Identifiers: chr3:g.148895640C>G (hg19) ; chr3:g.149177853C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177853C>G , CM000665.2:g.149177853C>G	GRCh38
NC_000003.11:g.148895640C>G , CM000665.1:g.148895640C>G	GRCh37
NC_000003.10:g.150378330C>G	NCBI36
NG_011800.1:g.49193G>C
NG_011800.2:g.49193G>C
NG_011800.3:g.49193G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.3005G>C MANE Select	ENSP00000264613.6:p.Ser1002Thr
ENST00000264613.10:c.3005G>C	ENSP00000264613.6:p.Ser1002Thr
ENST00000460674.5:n.922G>C
ENST00000463556.5:n.527G>C
ENST00000473296.1:n.55G>C
ENST00000479771.5:c.410G>C	ENSP00000420367.1:p.Ser137Thr
ENST00000481169.5:c.2792G>C	ENSP00000418773.1:p.Ser931Thr
ENST00000490639.5:n.3037G>C
ENST00000494544.1:c.2354G>C	ENSP00000420545.1:p.Ser785Thr
NM_000096.3:c.3005G>C	NP_000087.1:p.Ser1002Thr
NR_046371.1:n.3045G>C
XM_006713499.2:c.3005G>C	XP_006713562.1:p.Ser1002Thr
XM_006713500.2:c.3005G>C	XP_006713563.1:p.Ser1002Thr
XM_006713501.2:c.3005G>C	XP_006713564.1:p.Ser1002Thr
XM_011512435.1:c.3005G>C	XP_011510737.1:p.Ser1002Thr
XR_427361.2:n.3263G>C
XM_006713499.3:c.3005G>C	XP_006713562.1:p.Ser1002Thr
XM_006713500.4:c.3005G>C	XP_006713563.1:p.Ser1002Thr
XM_006713501.3:c.3005G>C	XP_006713564.1:p.Ser1002Thr
XM_011512435.2:c.3005G>C	XP_011510737.1:p.Ser1002Thr
XM_017005734.2:c.3005G>C	XP_016861223.1:p.Ser1002Thr
XM_017005735.2:c.3005G>C	XP_016861224.1:p.Ser1002Thr
XR_427361.3:n.3221G>C
NM_000096.4:c.3005G>C MANE Select	NP_000087.2:p.Ser1002Thr
NR_046371.2:n.2829G>C