Canonical Allele Identifier: CA405896842

Gene: PRX

Linked Data

• ClinVar Variation Id: 917237
• ClinVar RCV Id: RCV001173941
• dbSNP Id: rs1387072587
• gnomAD v2: 19-40902086-G-A
• gnomAD v4: 19-40396179-G-A
• MyVariant Identifiers: chr19:g.40902086G>A (hg19) ; chr19:g.40396179G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396179G>A , CM000681.2:g.40396179G>A	GRCh38
NC_000019.9:g.40902086G>A , CM000681.1:g.40902086G>A	GRCh37
NC_000019.8:g.45593926G>A	NCBI36
NG_007979.1:g.22186C>T , LRG_265:g.22186C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.2173C>T MANE Select	ENSP00000326018.6:p.Pro725Ser
ENST00000673881.1:c.1756C>T	ENSP00000501070.1:p.Pro586Ser
ENST00000674005.2:c.2458C>T	ENSP00000501261.1:p.Pro820Ser
ENST00000674773.1:c.1756C>T	ENSP00000502579.1:p.Pro586Ser
ENST00000675517.1:c.2048C>T
ENST00000676076.1:c.2034C>T
ENST00000676260.1:c.2135C>T
ENST00000676316.1:c.2060C>T
ENST00000291825.11:c.*2378C>T	ENSP00000291825.6:n.*2378C>T
ENST00000324001.7:c.2173C>T	ENSP00000326018.6:p.Pro725Ser
NM_020956.2:c.*2378C>T , LRG_265t1:c.*2378C>T	NP_066007.1:n.*2378C>T
NM_181882.2:c.2173C>T , LRG_265t2:c.2173C>T	NP_870998.2:p.Pro725Ser
XM_011527171.1:c.2173C>T	XP_011525473.1:p.Pro725Ser
XM_011527171.2:c.2173C>T	XP_011525473.1:p.Pro725Ser
XM_017027046.1:c.2071C>T	XP_016882535.1:p.Pro691Ser
XM_017027047.1:c.2071C>T	XP_016882536.1:p.Pro691Ser
NM_181882.3:c.2173C>T MANE Select	NP_870998.2:p.Pro725Ser