Canonical Allele Identifier: CA357790319

Gene: PPA2

Linked Data

• MyVariant Identifiers: chr4:g.106320204A>T (hg19) ; chr4:g.105399047A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105399047A>T , CM000666.2:g.105399047A>T	GRCh38
NC_000004.11:g.106320204A>T , CM000666.1:g.106320204A>T	GRCh37
NC_000004.10:g.106539653A>T	NCBI36
NG_053007.1:g.80024T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000341695.10:c.773T>A MANE Select	ENSP00000343885.5:p.Phe258Tyr
ENST00000341695.9:c.773T>A	ENSP00000343885.5:p.Phe258Tyr
ENST00000348706.9:c.686T>A	ENSP00000313061.8:p.Phe229Tyr
ENST00000351450.10:c.*495T>A	ENSP00000273977.9:n.*495T>A
ENST00000354147.7:c.275T>A	ENSP00000340352.3:p.Phe92Tyr
ENST00000432483.6:c.467T>A	ENSP00000389957.2:p.Phe156Tyr
ENST00000503171.5:n.465T>A
ENST00000509031.5:c.*532T>A	ENSP00000423467.1:n.*532T>A
ENST00000509426.5:n.782T>A
ENST00000510015.5:c.554T>A	ENSP00000423363.1:p.Phe185Tyr
ENST00000513605.5:n.590T>A
ENST00000515567.5:c.143-28174T>A
NM_006903.4:c.686T>A	NP_008834.3:p.Phe229Tyr
NM_176866.2:c.467T>A	NP_789842.2:p.Phe156Tyr
NM_176867.3:c.275T>A	NP_789843.2:p.Phe92Tyr
NM_176869.2:c.773T>A	NP_789845.1:p.Phe258Tyr
NM_176869.3:c.773T>A MANE Select	NP_789845.1:p.Phe258Tyr