Canonical Allele Identifier: CA9443867

Gene: PRX

Linked Data

• ClinVar Variation Id: 841612
• ClinVar RCV Id: RCV001043871
• dbSNP Id: rs750801377
• ExAC: 19:40900867 G / T
• gnomAD v2: 19-40900867-G-T
• gnomAD v3: 19-40394960-G-T
• gnomAD v4: 19-40394960-G-T
• MyVariant Identifiers: chr19:g.40900867G>T (hg19) ; chr19:g.40394960G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394960G>T , CM000681.2:g.40394960G>T	GRCh38
NC_000019.9:g.40900867G>T , CM000681.1:g.40900867G>T	GRCh37
NC_000019.8:g.45592707G>T	NCBI36
NG_007979.1:g.23405C>A , LRG_265:g.23405C>A
NG_051224.1:g.262C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3392C>A MANE Select	ENSP00000326018.6:p.Ala1131Asp
ENST00000673881.1:c.2975C>A	ENSP00000501070.1:p.Ala992Asp
ENST00000674005.2:c.3677C>A	ENSP00000501261.1:p.Ala1226Asp
ENST00000674773.1:c.2975C>A	ENSP00000502579.1:p.Ala992Asp
ENST00000675517.1:c.3267C>A
ENST00000676076.1:c.3253C>A
ENST00000676260.1:c.3354C>A
ENST00000676316.1:c.3279C>A
ENST00000291825.11:c.*3597C>A	ENSP00000291825.6:n.*3597C>A
ENST00000324001.7:c.3392C>A	ENSP00000326018.6:p.Ala1131Asp
NM_020956.2:c.*3597C>A , LRG_265t1:c.*3597C>A	NP_066007.1:n.*3597C>A
NM_181882.2:c.3392C>A , LRG_265t2:c.3392C>A	NP_870998.2:p.Ala1131Asp
XM_011527171.1:c.3392C>A	XP_011525473.1:p.Ala1131Asp
XM_011527171.2:c.3392C>A	XP_011525473.1:p.Ala1131Asp
XM_017027046.1:c.3290C>A	XP_016882535.1:p.Ala1097Asp
XM_017027047.1:c.3290C>A	XP_016882536.1:p.Ala1097Asp
NM_181882.3:c.3392C>A MANE Select	NP_870998.2:p.Ala1131Asp