Canonical Allele Identifier: CA1410105481
Gene: CP HGNC NCBI

Linked Data

dbSNP Id: rs1726206724

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149186755_149186760dup , CM000665.2:g.149186755_149186760dup GRCh38
NC_000003.11:g.148904542_148904547dup , CM000665.1:g.148904542_148904547dup GRCh37
NC_000003.10:g.150387232_150387237dup NCBI36
NG_011800.1:g.40286_40291dup
NG_011800.2:g.40286_40291dup
NG_011800.3:g.40286_40291dup

Transcript Alleles

HGVS Amino-acid change
ENST00000264613.11:c.1865-28_1865-23dup MANE Select ENSP00000264613.6:n.1865-28_1865-23dup
ENST00000264613.10:c.1865-28_1865-23dup ENSP00000264613.6:n.1865-28_1865-23dup
ENST00000462336.5:n.239-28_239-23dup
ENST00000481169.5:c.1864+1292_1864+1297dup ENSP00000418773.1:n.1864+1292_1864+1297dup
ENST00000489736.5:n.1090-28_1090-23dup
ENST00000490639.5:n.1897-28_1897-23dup
ENST00000494544.1:c.1214-28_1214-23dup ENSP00000420545.1:n.1214-28_1214-23dup
ENST00000497902.5:n.46-28_46-23dup
NM_000096.3:c.1865-28_1865-23dup NP_000087.1:n.1865-28_1865-23dup
NR_046371.1:n.2117+1292_2117+1297dup
XM_006713499.2:c.1865-28_1865-23dup XP_006713562.1:n.1865-28_1865-23dup
XM_006713500.2:c.1865-28_1865-23dup XP_006713563.1:n.1865-28_1865-23dup
XM_006713501.2:c.1865-28_1865-23dup XP_006713564.1:n.1865-28_1865-23dup
XM_006713502.2:c.1865-28_1865-23dup XP_006713565.1:n.1865-28_1865-23dup
XM_011512435.1:c.1865-28_1865-23dup XP_011510737.1:n.1865-28_1865-23dup
XR_427361.2:n.2123-28_2123-23dup
XM_006713499.3:c.1865-28_1865-23dup XP_006713562.1:n.1865-28_1865-23dup
XM_006713500.4:c.1865-28_1865-23dup XP_006713563.1:n.1865-28_1865-23dup
XM_006713501.3:c.1865-28_1865-23dup XP_006713564.1:n.1865-28_1865-23dup
XM_011512435.2:c.1865-28_1865-23dup XP_011510737.1:n.1865-28_1865-23dup
XM_017005734.2:c.1865-28_1865-23dup XP_016861223.1:n.1865-28_1865-23dup
XM_017005735.2:c.1865-28_1865-23dup XP_016861224.1:n.1865-28_1865-23dup
XR_427361.3:n.2081-28_2081-23dup
NM_000096.4:c.1865-28_1865-23dup MANE Select NP_000087.2:n.1865-28_1865-23dup
NR_046371.2:n.1901+1292_1901+1297dup