Canonical Allele Identifier: CA354930004

Gene: CP

Linked Data

• dbSNP Id: rs570400135
• MyVariant Identifiers: chr3:g.148897383C>G (hg19) ; chr3:g.149179596C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149179596C>G , CM000665.2:g.149179596C>G	GRCh38
NC_000003.11:g.148897383C>G , CM000665.1:g.148897383C>G	GRCh37
NC_000003.10:g.150380073C>G	NCBI36
NG_011800.1:g.47450G>C
NG_011800.2:g.47450G>C
NG_011800.3:g.47450G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000264613.11:c.2621G>C MANE Select	ENSP00000264613.6:p.Cys874Ser
ENST00000264613.10:c.2621G>C	ENSP00000264613.6:p.Cys874Ser
ENST00000460674.5:n.538G>C
ENST00000463556.5:n.143G>C
ENST00000479771.5:c.26G>C	ENSP00000420367.1:p.Cys9Ser
ENST00000481169.5:c.2408G>C	ENSP00000418773.1:p.Cys803Ser
ENST00000490639.5:n.2653G>C
ENST00000494544.1:c.1970G>C	ENSP00000420545.1:p.Cys657Ser
NM_000096.3:c.2621G>C	NP_000087.1:p.Cys874Ser
NR_046371.1:n.2661G>C
XM_006713499.2:c.2621G>C	XP_006713562.1:p.Cys874Ser
XM_006713500.2:c.2621G>C	XP_006713563.1:p.Cys874Ser
XM_006713501.2:c.2621G>C	XP_006713564.1:p.Cys874Ser
XM_006713502.2:c.2621G>C	XP_006713565.1:p.Cys874Ser
XM_011512435.1:c.2621G>C	XP_011510737.1:p.Cys874Ser
XR_427361.2:n.2879G>C
XM_006713499.3:c.2621G>C	XP_006713562.1:p.Cys874Ser
XM_006713500.4:c.2621G>C	XP_006713563.1:p.Cys874Ser
XM_006713501.3:c.2621G>C	XP_006713564.1:p.Cys874Ser
XM_011512435.2:c.2621G>C	XP_011510737.1:p.Cys874Ser
XM_017005734.2:c.2621G>C	XP_016861223.1:p.Cys874Ser
XM_017005735.2:c.2621G>C	XP_016861224.1:p.Cys874Ser
XR_427361.3:n.2837G>C
NM_000096.4:c.2621G>C MANE Select	NP_000087.2:p.Cys874Ser
NR_046371.2:n.2445G>C