Canonical Allele Identifier: CA357790297
Gene: PPA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.105399044T>G , CM000666.2:g.105399044T>G GRCh38
NC_000004.11:g.106320201T>G , CM000666.1:g.106320201T>G GRCh37
NC_000004.10:g.106539650T>G NCBI36
NG_053007.1:g.80027A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000341695.10:c.776A>C MANE Select ENSP00000343885.5:p.Lys259Thr
ENST00000341695.9:c.776A>C ENSP00000343885.5:p.Lys259Thr
ENST00000348706.9:c.689A>C ENSP00000313061.8:p.Lys230Thr
ENST00000351450.10:c.*498A>C ENSP00000273977.9:n.*498A>C
ENST00000354147.7:c.278A>C ENSP00000340352.3:p.Lys93Thr
ENST00000432483.6:c.470A>C ENSP00000389957.2:p.Lys157Thr
ENST00000503171.5:n.468A>C
ENST00000509031.5:c.*535A>C ENSP00000423467.1:n.*535A>C
ENST00000509426.5:n.785A>C
ENST00000510015.5:c.557A>C ENSP00000423363.1:p.Lys186Thr
ENST00000513605.5:n.593A>C
ENST00000515567.5:c.143-28171A>C
NM_006903.4:c.689A>C NP_008834.3:p.Lys230Thr
NM_176866.2:c.470A>C NP_789842.2:p.Lys157Thr
NM_176867.3:c.278A>C NP_789843.2:p.Lys93Thr
NM_176869.2:c.776A>C NP_789845.1:p.Lys259Thr
NM_176869.3:c.776A>C MANE Select NP_789845.1:p.Lys259Thr