Canonical Allele Identifier: CA354912850

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149206227C>T , CM000665.2:g.149206227C>T	GRCh38
NC_000003.11:g.148924014C>T , CM000665.1:g.148924014C>T	GRCh37
NC_000003.10:g.150406704C>T	NCBI36
NG_011800.1:g.20819G>A
NG_011800.2:g.20819G>A
NG_011800.3:g.20819G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000096.4:c.1149G>A MANE Select	NP_000087.2:p.Trp383Ter
ENST00000264613.11:c.1149G>A MANE Select	ENSP00000264613.6:p.Trp383Ter
NM_000096.3:c.1149G>A	NP_000087.1:p.Trp383Ter
NR_046371.1:n.1402G>A
NR_046371.2:n.1186G>A
ENST00000264613.10:c.1149G>A	ENSP00000264613.6:p.Trp383Ter
ENST00000481169.5:c.1149G>A	ENSP00000418773.1:p.Trp383Ter
ENST00000489736.5:n.374G>A
ENST00000490639.5:n.1181G>A
ENST00000494544.1:c.498G>A	ENSP00000420545.1:p.Trp166Ter
XM_006713499.2:c.1149G>A	XP_006713562.1:p.Trp383Ter
XM_006713499.3:c.1149G>A	XP_006713562.1:p.Trp383Ter
XM_006713500.2:c.1149G>A	XP_006713563.1:p.Trp383Ter
XM_006713500.4:c.1149G>A	XP_006713563.1:p.Trp383Ter
XM_006713501.2:c.1149G>A	XP_006713564.1:p.Trp383Ter
XM_006713501.3:c.1149G>A	XP_006713564.1:p.Trp383Ter
XM_006713502.2:c.1149G>A	XP_006713565.1:p.Trp383Ter
XM_011512435.1:c.1149G>A	XP_011510737.1:p.Trp383Ter
XM_011512435.2:c.1149G>A	XP_011510737.1:p.Trp383Ter
XM_017005734.2:c.1149G>A	XP_016861223.1:p.Trp383Ter
XM_017005735.2:c.1149G>A	XP_016861224.1:p.Trp383Ter
XR_427361.2:n.1407G>A
XR_427361.3:n.1365G>A