Canonical Allele Identifier: CA357790262

Gene: PPA2

Linked Data

• MyVariant Identifiers: chr4:g.106320196T>G (hg19) ; chr4:g.105399039T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105399039T>G , CM000666.2:g.105399039T>G	GRCh38
NC_000004.11:g.106320196T>G , CM000666.1:g.106320196T>G	GRCh37
NC_000004.10:g.106539645T>G	NCBI36
NG_053007.1:g.80032A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000341695.10:c.781A>C MANE Select	ENSP00000343885.5:p.Lys261Gln
ENST00000341695.9:c.781A>C	ENSP00000343885.5:p.Lys261Gln
ENST00000348706.9:c.694A>C	ENSP00000313061.8:p.Lys232Gln
ENST00000351450.10:c.*503A>C	ENSP00000273977.9:n.*503A>C
ENST00000354147.7:c.283A>C	ENSP00000340352.3:p.Lys95Gln
ENST00000432483.6:c.475A>C	ENSP00000389957.2:p.Lys159Gln
ENST00000503171.5:n.473A>C
ENST00000509031.5:c.*540A>C	ENSP00000423467.1:n.*540A>C
ENST00000509426.5:n.790A>C
ENST00000510015.5:c.562A>C	ENSP00000423363.1:p.Lys188Gln
ENST00000513605.5:n.598A>C
ENST00000515567.5:c.143-28166A>C
NM_006903.4:c.694A>C	NP_008834.3:p.Lys232Gln
NM_176866.2:c.475A>C	NP_789842.2:p.Lys159Gln
NM_176867.3:c.283A>C	NP_789843.2:p.Lys95Gln
NM_176869.2:c.781A>C	NP_789845.1:p.Lys261Gln
NM_176869.3:c.781A>C MANE Select	NP_789845.1:p.Lys261Gln