Canonical Allele Identifier: CA357790280
Gene: PPA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105399043T>A , CM000666.2:g.105399043T>A GRCh38
NC_000004.11:g.106320200T>A , CM000666.1:g.106320200T>A GRCh37
NC_000004.10:g.106539649T>A NCBI36
NG_053007.1:g.80028A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000341695.10:c.777A>T MANE Select ENSP00000343885.5:p.Lys259Asn
ENST00000341695.9:c.777A>T ENSP00000343885.5:p.Lys259Asn
ENST00000348706.9:c.690A>T ENSP00000313061.8:p.Lys230Asn
ENST00000351450.10:c.*499A>T ENSP00000273977.9:n.*499A>T
ENST00000354147.7:c.279A>T ENSP00000340352.3:p.Lys93Asn
ENST00000432483.6:c.471A>T ENSP00000389957.2:p.Lys157Asn
ENST00000503171.5:n.469A>T
ENST00000509031.5:c.*536A>T ENSP00000423467.1:n.*536A>T
ENST00000509426.5:n.786A>T
ENST00000510015.5:c.558A>T ENSP00000423363.1:p.Lys186Asn
ENST00000513605.5:n.594A>T
ENST00000515567.5:c.143-28170A>T
NM_006903.4:c.690A>T NP_008834.3:p.Lys230Asn
NM_176866.2:c.471A>T NP_789842.2:p.Lys157Asn
NM_176867.3:c.279A>T NP_789843.2:p.Lys93Asn
NM_176869.2:c.777A>T NP_789845.1:p.Lys259Asn
NM_176869.3:c.777A>T MANE Select NP_789845.1:p.Lys259Asn