Canonical Allele Identifier: CA2668139337
Gene: CP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149186145_149186148dup , CM000665.2:g.149186145_149186148dup GRCh38
NC_000003.11:g.148903932_148903935dup , CM000665.1:g.148903932_148903935dup GRCh37
NC_000003.10:g.150386622_150386625dup NCBI36
NG_011800.1:g.40899_40902dup
NG_011800.2:g.40899_40902dup
NG_011800.3:g.40899_40902dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000264613.11:c.2077+373_2077+376dup MANE Select ENSP00000264613.6:n.2077+373_2077+376dup
ENST00000264613.10:c.2077+373_2077+376dup ENSP00000264613.6:n.2077+373_2077+376dup
ENST00000462336.5:n.451+373_451+376dup
ENST00000481169.5:c.1865-701_1865-698dup ENSP00000418773.1:n.1865-701_1865-698dup
ENST00000489736.5:n.1675_1678dup
ENST00000490639.5:n.2109+373_2109+376dup
ENST00000494544.1:c.1426+373_1426+376dup ENSP00000420545.1:n.1426+373_1426+376dup
ENST00000497902.5:n.258+373_258+376dup
NM_000096.3:c.2077+373_2077+376dup NP_000087.1:n.2077+373_2077+376dup
NR_046371.1:n.2118-701_2118-698dup
XM_006713499.2:c.2077+373_2077+376dup XP_006713562.1:n.2077+373_2077+376dup
XM_006713500.2:c.2077+373_2077+376dup XP_006713563.1:n.2077+373_2077+376dup
XM_006713501.2:c.2077+373_2077+376dup XP_006713564.1:n.2077+373_2077+376dup
XM_006713502.2:c.2077+373_2077+376dup XP_006713565.1:n.2077+373_2077+376dup
XM_011512435.1:c.2077+373_2077+376dup XP_011510737.1:n.2077+373_2077+376dup
XR_427361.2:n.2335+373_2335+376dup
XM_006713499.3:c.2077+373_2077+376dup XP_006713562.1:n.2077+373_2077+376dup
XM_006713500.4:c.2077+373_2077+376dup XP_006713563.1:n.2077+373_2077+376dup
XM_006713501.3:c.2077+373_2077+376dup XP_006713564.1:n.2077+373_2077+376dup
XM_011512435.2:c.2077+373_2077+376dup XP_011510737.1:n.2077+373_2077+376dup
XM_017005734.2:c.2077+373_2077+376dup XP_016861223.1:n.2077+373_2077+376dup
XM_017005735.2:c.2077+373_2077+376dup XP_016861224.1:n.2077+373_2077+376dup
XR_427361.3:n.2293+373_2293+376dup
NM_000096.4:c.2077+373_2077+376dup MANE Select NP_000087.2:n.2077+373_2077+376dup
NR_046371.2:n.1902-701_1902-698dup