Canonical Allele Identifier: CA2758856132

Gene: CP

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149177918del , CM000665.2:g.149177918del	GRCh38
NC_000003.11:g.148895705del , CM000665.1:g.148895705del	GRCh37
NC_000003.10:g.150378395del	NCBI36
NG_011800.1:g.49128del
NG_011800.2:g.49128del
NG_011800.3:g.49128del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.2940del MANE Select	ENSP00000264613.6:p.Asn981ThrfsTer4
ENST00000264613.10:c.2940del	ENSP00000264613.6:p.Asn981ThrfsTer4
ENST00000460674.5:n.857del
ENST00000463556.5:n.462del
ENST00000479771.5:c.345del	ENSP00000420367.1:p.Asn116ThrfsTer4
ENST00000481169.5:c.2727del	ENSP00000418773.1:p.Asn910ThrfsTer4
ENST00000490639.5:n.2972del
ENST00000494544.1:c.2289del	ENSP00000420545.1:p.Asn764ThrfsTer4
NM_000096.3:c.2940del	NP_000087.1:p.Asn981ThrfsTer4
NR_046371.1:n.2980del
XM_006713499.2:c.2940del	XP_006713562.1:p.Asn981ThrfsTer4
XM_006713500.2:c.2940del	XP_006713563.1:p.Asn981ThrfsTer4
XM_006713501.2:c.2940del	XP_006713564.1:p.Asn981ThrfsTer4
XM_011512435.1:c.2940del	XP_011510737.1:p.Asn981ThrfsTer4
XR_427361.2:n.3198del
XM_006713499.3:c.2940del	XP_006713562.1:p.Asn981ThrfsTer4
XM_006713500.4:c.2940del	XP_006713563.1:p.Asn981ThrfsTer4
XM_006713501.3:c.2940del	XP_006713564.1:p.Asn981ThrfsTer4
XM_011512435.2:c.2940del	XP_011510737.1:p.Asn981ThrfsTer4
XM_017005734.2:c.2940del	XP_016861223.1:p.Asn981ThrfsTer4
XM_017005735.2:c.2940del	XP_016861224.1:p.Asn981ThrfsTer4
XR_427361.3:n.3156del
NM_000096.4:c.2940del MANE Select	NP_000087.2:p.Asn981ThrfsTer4
NR_046371.2:n.2764del