Canonical Allele Identifier: CA354930000
Gene: CP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149179595A>T , CM000665.2:g.149179595A>T GRCh38
NC_000003.11:g.148897382A>T , CM000665.1:g.148897382A>T GRCh37
NC_000003.10:g.150380072A>T NCBI36
NG_011800.1:g.47451T>A
NG_011800.2:g.47451T>A
NG_011800.3:g.47451T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000264613.11:c.2622T>A MANE Select ENSP00000264613.6:p.Cys874Ter
ENST00000264613.10:c.2622T>A ENSP00000264613.6:p.Cys874Ter
ENST00000460674.5:n.539T>A
ENST00000463556.5:n.144T>A
ENST00000479771.5:c.27T>A ENSP00000420367.1:p.Cys9Ter
ENST00000481169.5:c.2409T>A ENSP00000418773.1:p.Cys803Ter
ENST00000490639.5:n.2654T>A
ENST00000494544.1:c.1971T>A ENSP00000420545.1:p.Cys657Ter
NM_000096.3:c.2622T>A NP_000087.1:p.Cys874Ter
NR_046371.1:n.2662T>A
XM_006713499.2:c.2622T>A XP_006713562.1:p.Cys874Ter
XM_006713500.2:c.2622T>A XP_006713563.1:p.Cys874Ter
XM_006713501.2:c.2622T>A XP_006713564.1:p.Cys874Ter
XM_006713502.2:c.2622T>A XP_006713565.1:p.Cys874Ter
XM_011512435.1:c.2622T>A XP_011510737.1:p.Cys874Ter
XR_427361.2:n.2880T>A
XM_006713499.3:c.2622T>A XP_006713562.1:p.Cys874Ter
XM_006713500.4:c.2622T>A XP_006713563.1:p.Cys874Ter
XM_006713501.3:c.2622T>A XP_006713564.1:p.Cys874Ter
XM_011512435.2:c.2622T>A XP_011510737.1:p.Cys874Ter
XM_017005734.2:c.2622T>A XP_016861223.1:p.Cys874Ter
XM_017005735.2:c.2622T>A XP_016861224.1:p.Cys874Ter
XR_427361.3:n.2838T>A
NM_000096.4:c.2622T>A MANE Select NP_000087.2:p.Cys874Ter
NR_046371.2:n.2446T>A