Canonical Allele Identifier: CA357790266

Gene: PPA2

Linked Data

• MyVariant Identifiers: chr4:g.106320198T>G (hg19) ; chr4:g.105399041T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.105399041T>G , CM000666.2:g.105399041T>G	GRCh38
NC_000004.11:g.106320198T>G , CM000666.1:g.106320198T>G	GRCh37
NC_000004.10:g.106539647T>G	NCBI36
NG_053007.1:g.80030A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000341695.10:c.779A>C MANE Select	ENSP00000343885.5:p.Asn260Thr
ENST00000341695.9:c.779A>C	ENSP00000343885.5:p.Asn260Thr
ENST00000348706.9:c.692A>C	ENSP00000313061.8:p.Asn231Thr
ENST00000351450.10:c.*501A>C	ENSP00000273977.9:n.*501A>C
ENST00000354147.7:c.281A>C	ENSP00000340352.3:p.Asn94Thr
ENST00000432483.6:c.473A>C	ENSP00000389957.2:p.Asn158Thr
ENST00000503171.5:n.471A>C
ENST00000509031.5:c.*538A>C	ENSP00000423467.1:n.*538A>C
ENST00000509426.5:n.788A>C
ENST00000510015.5:c.560A>C	ENSP00000423363.1:p.Asn187Thr
ENST00000513605.5:n.596A>C
ENST00000515567.5:c.143-28168A>C
NM_006903.4:c.692A>C	NP_008834.3:p.Asn231Thr
NM_176866.2:c.473A>C	NP_789842.2:p.Asn158Thr
NM_176867.3:c.281A>C	NP_789843.2:p.Asn94Thr
NM_176869.2:c.779A>C	NP_789845.1:p.Asn260Thr
NM_176869.3:c.779A>C MANE Select	NP_789845.1:p.Asn260Thr