Canonical Allele Identifier: CA354930949
Gene: CP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.149182084T>G , CM000665.2:g.149182084T>G GRCh38
NC_000003.11:g.148899871T>G , CM000665.1:g.148899871T>G GRCh37
NC_000003.10:g.150382561T>G NCBI36
NG_011800.1:g.44962A>C
NG_011800.2:g.44962A>C
NG_011800.3:g.44962A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264613.11:c.2475A>C MANE Select ENSP00000264613.6:p.Lys825Asn
ENST00000264613.10:c.2475A>C ENSP00000264613.6:p.Lys825Asn
ENST00000481169.5:c.2262A>C ENSP00000418773.1:p.Lys754Asn
ENST00000490639.5:n.2507A>C
ENST00000494544.1:c.1824A>C ENSP00000420545.1:p.Lys608Asn
NM_000096.3:c.2475A>C NP_000087.1:p.Lys825Asn
NR_046371.1:n.2515A>C
XM_006713499.2:c.2475A>C XP_006713562.1:p.Lys825Asn
XM_006713500.2:c.2475A>C XP_006713563.1:p.Lys825Asn
XM_006713501.2:c.2475A>C XP_006713564.1:p.Lys825Asn
XM_006713502.2:c.2475A>C XP_006713565.1:p.Lys825Asn
XM_011512435.1:c.2475A>C XP_011510737.1:p.Lys825Asn
XR_427361.2:n.2733A>C
XM_006713499.3:c.2475A>C XP_006713562.1:p.Lys825Asn
XM_006713500.4:c.2475A>C XP_006713563.1:p.Lys825Asn
XM_006713501.3:c.2475A>C XP_006713564.1:p.Lys825Asn
XM_011512435.2:c.2475A>C XP_011510737.1:p.Lys825Asn
XM_017005734.2:c.2475A>C XP_016861223.1:p.Lys825Asn
XM_017005735.2:c.2475A>C XP_016861224.1:p.Lys825Asn
XR_427361.3:n.2691A>C
NM_000096.4:c.2475A>C MANE Select NP_000087.2:p.Lys825Asn
NR_046371.2:n.2299A>C