Canonical Allele Identifier: CA2660740
Gene: CP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149182034T>C , CM000665.2:g.149182034T>C GRCh38
NC_000003.11:g.148899821T>C , CM000665.1:g.148899821T>C GRCh37
NC_000003.10:g.150382511T>C NCBI36
NG_011800.1:g.45012A>G
NG_011800.2:g.45012A>G
NG_011800.3:g.45012A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000096.4:c.2525A>G MANE Select NP_000087.2:p.Glu842Gly
ENST00000264613.11:c.2525A>G MANE Select ENSP00000264613.6:p.Glu842Gly
NM_000096.3:c.2525A>G NP_000087.1:p.Glu842Gly
NR_046371.1:n.2565A>G
NR_046371.2:n.2349A>G
ENST00000264613.10:c.2525A>G ENSP00000264613.6:p.Glu842Gly
ENST00000481169.5:c.2312A>G ENSP00000418773.1:p.Glu771Gly
ENST00000490639.5:n.2557A>G
ENST00000494544.1:c.1874A>G ENSP00000420545.1:p.Glu625Gly
XM_006713499.2:c.2525A>G XP_006713562.1:p.Glu842Gly
XM_006713499.3:c.2525A>G XP_006713562.1:p.Glu842Gly
XM_006713500.2:c.2525A>G XP_006713563.1:p.Glu842Gly
XM_006713500.4:c.2525A>G XP_006713563.1:p.Glu842Gly
XM_006713501.2:c.2525A>G XP_006713564.1:p.Glu842Gly
XM_006713501.3:c.2525A>G XP_006713564.1:p.Glu842Gly
XM_006713502.2:c.2525A>G XP_006713565.1:p.Glu842Gly
XM_011512435.1:c.2525A>G XP_011510737.1:p.Glu842Gly
XM_011512435.2:c.2525A>G XP_011510737.1:p.Glu842Gly
XM_017005734.2:c.2525A>G XP_016861223.1:p.Glu842Gly
XM_017005735.2:c.2525A>G XP_016861224.1:p.Glu842Gly
XR_427361.2:n.2783A>G
XR_427361.3:n.2741A>G