Canonical Allele Identifier: CA436218299
Gene: CP HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.148904431A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149186644A>G , CM000665.2:g.149186644A>G GRCh38
NC_000003.11:g.148904431A>G , CM000665.1:g.148904431A>G GRCh37
NC_000003.10:g.150387121A>G NCBI36
NG_011800.1:g.40402T>C
NG_011800.2:g.40402T>C
NG_011800.3:g.40402T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264613.11:c.1953T>C MANE Select ENSP00000264613.6:p.Asn651=
ENST00000264613.10:c.1953T>C ENSP00000264613.6:p.Asn651=
ENST00000462336.5:n.327T>C
ENST00000481169.5:c.1865-1198T>C ENSP00000418773.1:n.1865-1198T>C
ENST00000489736.5:n.1178T>C
ENST00000490639.5:n.1985T>C
ENST00000494544.1:c.1302T>C ENSP00000420545.1:p.Asn434=
ENST00000497902.5:n.134T>C
NM_000096.3:c.1953T>C NP_000087.1:p.Asn651=
NR_046371.1:n.2118-1198T>C
XM_006713499.2:c.1953T>C XP_006713562.1:p.Asn651=
XM_006713500.2:c.1953T>C XP_006713563.1:p.Asn651=
XM_006713501.2:c.1953T>C XP_006713564.1:p.Asn651=
XM_006713502.2:c.1953T>C XP_006713565.1:p.Asn651=
XM_011512435.1:c.1953T>C XP_011510737.1:p.Asn651=
XR_427361.2:n.2211T>C
XM_006713499.3:c.1953T>C XP_006713562.1:p.Asn651=
XM_006713500.4:c.1953T>C XP_006713563.1:p.Asn651=
XM_006713501.3:c.1953T>C XP_006713564.1:p.Asn651=
XM_011512435.2:c.1953T>C XP_011510737.1:p.Asn651=
XM_017005734.2:c.1953T>C XP_016861223.1:p.Asn651=
XM_017005735.2:c.1953T>C XP_016861224.1:p.Asn651=
XR_427361.3:n.2169T>C
NM_000096.4:c.1953T>C MANE Select NP_000087.2:p.Asn651=
NR_046371.2:n.1902-1198T>C