Canonical Allele Identifier: CA3032573

Gene: PPA2

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105446478G>A , CM000666.2:g.105446478G>A	GRCh38
NC_000004.11:g.106367635G>A , CM000666.1:g.106367635G>A	GRCh37
NC_000004.10:g.106587084G>A	NCBI36
NG_053007.1:g.32593C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_176869.3:c.346C>T MANE Select	NP_789845.1:p.Pro116Ser
ENST00000341695.10:c.346C>T MANE Select	ENSP00000343885.5:p.Pro116Ser
NM_006903.4:c.346C>T	NP_008834.3:p.Pro116Ser
NM_176866.2:c.222+10203C>T	NP_789842.2:n.222+10203C>T
NM_176867.3:c.157+27416C>T	NP_789843.2:n.157+27416C>T
NM_176869.2:c.346C>T	NP_789845.1:p.Pro116Ser
ENST00000341695.9:c.346C>T	ENSP00000343885.5:p.Pro116Ser
ENST00000348706.9:c.346C>T	ENSP00000313061.8:p.Pro116Ser
ENST00000351450.10:c.*68C>T	ENSP00000273977.9:n.*68C>T
ENST00000354147.7:c.157+27416C>T	ENSP00000340352.3:n.157+27416C>T
ENST00000432483.6:c.222+10203C>T	ENSP00000389957.2:n.222+10203C>T
ENST00000457404.6:n.358C>T
ENST00000499847.6:n.355C>T
ENST00000502596.5:c.109C>T	ENSP00000426347.1:p.Pro37Ser
ENST00000502833.5:n.355C>T
ENST00000503171.5:n.252C>T
ENST00000504028.5:c.331C>T	ENSP00000421177.1:p.Pro111Ser
ENST00000506815.5:c.218C>T	ENSP00000422405.1:n.218C>T
ENST00000508518.5:c.282C>T
ENST00000509031.5:c.*105C>T	ENSP00000423467.1:n.*105C>T
ENST00000509426.5:n.355C>T
ENST00000510015.5:c.223-8442C>T	ENSP00000423363.1:n.223-8442C>T
ENST00000513649.1:c.*103C>T	ENSP00000422738.1:n.*103C>T
ENST00000514209.5:c.*68C>T	ENSP00000424988.1:n.*68C>T
ENST00000515567.5:c.47C>T