Canonical Allele Identifier: CA645525203

Gene: CP

Linked Data

• COSMIC: COSM4449232

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.149186729del , CM000665.2:g.149186729del	GRCh38
NC_000003.11:g.148904516del , CM000665.1:g.148904516del	GRCh37
NC_000003.10:g.150387206del	NCBI36
NG_011800.1:g.40317del
NG_011800.2:g.40317del
NG_011800.3:g.40317del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264613.11:c.1868del MANE Select	ENSP00000264613.6:p.Met623ArgfsTer?
ENST00000264613.10:c.1868del	ENSP00000264613.6:p.Met623ArgfsTer?
ENST00000462336.5:n.242del
ENST00000481169.5:c.1865-1283del	ENSP00000418773.1:n.1865-1283del
ENST00000489736.5:n.1093del
ENST00000490639.5:n.1900del
ENST00000494544.1:c.1217del	ENSP00000420545.1:p.Met406ArgfsTer?
ENST00000497902.5:n.49del
NM_000096.3:c.1868del	NP_000087.1:p.Met623ArgfsTer?
NR_046371.1:n.2118-1283del
XM_006713499.2:c.1868del	XP_006713562.1:p.Met623ArgfsTer?
XM_006713500.2:c.1868del	XP_006713563.1:p.Met623ArgfsTer?
XM_006713501.2:c.1868del	XP_006713564.1:p.Met623ArgfsTer?
XM_006713502.2:c.1868del	XP_006713565.1:p.Met623ArgfsTer?
XM_011512435.1:c.1868del	XP_011510737.1:p.Met623ArgfsTer?
XR_427361.2:n.2126del
XM_006713499.3:c.1868del	XP_006713562.1:p.Met623ArgfsTer?
XM_006713500.4:c.1868del	XP_006713563.1:p.Met623ArgfsTer?
XM_006713501.3:c.1868del	XP_006713564.1:p.Met623ArgfsTer?
XM_011512435.2:c.1868del	XP_011510737.1:p.Met623ArgfsTer?
XM_017005734.2:c.1868del	XP_016861223.1:p.Met623ArgfsTer?
XM_017005735.2:c.1868del	XP_016861224.1:p.Met623ArgfsTer?
XR_427361.3:n.2084del
NM_000096.4:c.1868del MANE Select	NP_000087.2:p.Met623ArgfsTer?
NR_046371.2:n.1902-1283del