Canonical Allele Identifier: CA2668139504
Gene: CP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149186329_149186333del , CM000665.2:g.149186329_149186333del GRCh38
NC_000003.11:g.148904116_148904120del , CM000665.1:g.148904116_148904120del GRCh37
NC_000003.10:g.150386806_150386810del NCBI36
NG_011800.1:g.40713_40717del
NG_011800.2:g.40713_40717del
NG_011800.3:g.40713_40717del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264613.11:c.2077+187_2077+191del MANE Select ENSP00000264613.6:n.2077+187_2077+191del
ENST00000264613.10:c.2077+187_2077+191del ENSP00000264613.6:n.2077+187_2077+191del
ENST00000462336.5:n.451+187_451+191del
ENST00000481169.5:c.1865-887_1865-883del ENSP00000418773.1:n.1865-887_1865-883del
ENST00000489736.5:n.1489_1493del
ENST00000490639.5:n.2109+187_2109+191del
ENST00000494544.1:c.1426+187_1426+191del ENSP00000420545.1:n.1426+187_1426+191del
ENST00000497902.5:n.258+187_258+191del
NM_000096.3:c.2077+187_2077+191del NP_000087.1:n.2077+187_2077+191del
NR_046371.1:n.2118-887_2118-883del
XM_006713499.2:c.2077+187_2077+191del XP_006713562.1:n.2077+187_2077+191del
XM_006713500.2:c.2077+187_2077+191del XP_006713563.1:n.2077+187_2077+191del
XM_006713501.2:c.2077+187_2077+191del XP_006713564.1:n.2077+187_2077+191del
XM_006713502.2:c.2077+187_2077+191del XP_006713565.1:n.2077+187_2077+191del
XM_011512435.1:c.2077+187_2077+191del XP_011510737.1:n.2077+187_2077+191del
XR_427361.2:n.2335+187_2335+191del
XM_006713499.3:c.2077+187_2077+191del XP_006713562.1:n.2077+187_2077+191del
XM_006713500.4:c.2077+187_2077+191del XP_006713563.1:n.2077+187_2077+191del
XM_006713501.3:c.2077+187_2077+191del XP_006713564.1:n.2077+187_2077+191del
XM_011512435.2:c.2077+187_2077+191del XP_011510737.1:n.2077+187_2077+191del
XM_017005734.2:c.2077+187_2077+191del XP_016861223.1:n.2077+187_2077+191del
XM_017005735.2:c.2077+187_2077+191del XP_016861224.1:n.2077+187_2077+191del
XR_427361.3:n.2293+187_2293+191del
NM_000096.4:c.2077+187_2077+191del MANE Select NP_000087.2:n.2077+187_2077+191del
NR_046371.2:n.1902-887_1902-883del