Canonical Allele Identifier: CA354932702
Gene: CP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149186725A>T , CM000665.2:g.149186725A>T GRCh38
NC_000003.11:g.148904512A>T , CM000665.1:g.148904512A>T GRCh37
NC_000003.10:g.150387202A>T NCBI36
NG_011800.1:g.40321T>A
NG_011800.2:g.40321T>A
NG_011800.3:g.40321T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000264613.11:c.1872T>A MANE Select ENSP00000264613.6:p.Asn624Lys
ENST00000264613.10:c.1872T>A ENSP00000264613.6:p.Asn624Lys
ENST00000462336.5:n.246T>A
ENST00000481169.5:c.1865-1279T>A ENSP00000418773.1:n.1865-1279T>A
ENST00000489736.5:n.1097T>A
ENST00000490639.5:n.1904T>A
ENST00000494544.1:c.1221T>A ENSP00000420545.1:p.Asn407Lys
ENST00000497902.5:n.53T>A
NM_000096.3:c.1872T>A NP_000087.1:p.Asn624Lys
NR_046371.1:n.2118-1279T>A
XM_006713499.2:c.1872T>A XP_006713562.1:p.Asn624Lys
XM_006713500.2:c.1872T>A XP_006713563.1:p.Asn624Lys
XM_006713501.2:c.1872T>A XP_006713564.1:p.Asn624Lys
XM_006713502.2:c.1872T>A XP_006713565.1:p.Asn624Lys
XM_011512435.1:c.1872T>A XP_011510737.1:p.Asn624Lys
XR_427361.2:n.2130T>A
XM_006713499.3:c.1872T>A XP_006713562.1:p.Asn624Lys
XM_006713500.4:c.1872T>A XP_006713563.1:p.Asn624Lys
XM_006713501.3:c.1872T>A XP_006713564.1:p.Asn624Lys
XM_011512435.2:c.1872T>A XP_011510737.1:p.Asn624Lys
XM_017005734.2:c.1872T>A XP_016861223.1:p.Asn624Lys
XM_017005735.2:c.1872T>A XP_016861224.1:p.Asn624Lys
XR_427361.3:n.2088T>A
NM_000096.4:c.1872T>A MANE Select NP_000087.2:p.Asn624Lys
NR_046371.2:n.1902-1279T>A