Canonical Allele Identifier: CA2668137540
Gene: CP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149181979_149181981dup , CM000665.2:g.149181979_149181981dup GRCh38
NC_000003.11:g.148899766_148899768dup , CM000665.1:g.148899766_148899768dup GRCh37
NC_000003.10:g.150382456_150382458dup NCBI36
NG_011800.1:g.45069_45071dup
NG_011800.2:g.45069_45071dup
NG_011800.3:g.45069_45071dup

Transcript Alleles

HGVS Amino-acid change
ENST00000264613.11:c.2554+28_2554+30dup MANE Select ENSP00000264613.6:n.2554+28_2554+30dup
ENST00000264613.10:c.2554+28_2554+30dup ENSP00000264613.6:n.2554+28_2554+30dup
ENST00000481169.5:c.2341+28_2341+30dup ENSP00000418773.1:n.2341+28_2341+30dup
ENST00000490639.5:n.2586+28_2586+30dup
ENST00000494544.1:c.1903+28_1903+30dup ENSP00000420545.1:n.1903+28_1903+30dup
NM_000096.3:c.2554+28_2554+30dup NP_000087.1:n.2554+28_2554+30dup
NR_046371.1:n.2594+28_2594+30dup
XM_006713499.2:c.2554+28_2554+30dup XP_006713562.1:n.2554+28_2554+30dup
XM_006713500.2:c.2554+28_2554+30dup XP_006713563.1:n.2554+28_2554+30dup
XM_006713501.2:c.2554+28_2554+30dup XP_006713564.1:n.2554+28_2554+30dup
XM_006713502.2:c.2554+28_2554+30dup XP_006713565.1:n.2554+28_2554+30dup
XM_011512435.1:c.2554+28_2554+30dup XP_011510737.1:n.2554+28_2554+30dup
XR_427361.2:n.2812+28_2812+30dup
XM_006713499.3:c.2554+28_2554+30dup XP_006713562.1:n.2554+28_2554+30dup
XM_006713500.4:c.2554+28_2554+30dup XP_006713563.1:n.2554+28_2554+30dup
XM_006713501.3:c.2554+28_2554+30dup XP_006713564.1:n.2554+28_2554+30dup
XM_011512435.2:c.2554+28_2554+30dup XP_011510737.1:n.2554+28_2554+30dup
XM_017005734.2:c.2554+28_2554+30dup XP_016861223.1:n.2554+28_2554+30dup
XM_017005735.2:c.2554+28_2554+30dup XP_016861224.1:n.2554+28_2554+30dup
XR_427361.3:n.2770+28_2770+30dup
NM_000096.4:c.2554+28_2554+30dup MANE Select NP_000087.2:n.2554+28_2554+30dup
NR_046371.2:n.2378+28_2378+30dup