Canonical Allele Identifier: CA507679569

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40902225A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396318A>G , CM000681.2:g.40396318A>G	GRCh38
NC_000019.9:g.40902225A>G , CM000681.1:g.40902225A>G	GRCh37
NC_000019.8:g.45594065A>G	NCBI36
NG_007979.1:g.22047T>C , LRG_265:g.22047T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.2034T>C MANE Select	ENSP00000326018.6:p.Val678=
ENST00000673881.1:c.1617T>C	ENSP00000501070.1:p.Val539=
ENST00000674005.2:c.2319T>C	ENSP00000501261.1:p.Val773=
ENST00000674773.1:c.1617T>C	ENSP00000502579.1:p.Val539=
ENST00000675517.1:c.1909T>C
ENST00000676076.1:c.1895T>C
ENST00000676260.1:c.1996T>C
ENST00000676316.1:c.1921T>C
ENST00000291825.11:c.*2239T>C	ENSP00000291825.6:n.*2239T>C
ENST00000324001.7:c.2034T>C	ENSP00000326018.6:p.Val678=
NM_020956.2:c.*2239T>C , LRG_265t1:c.*2239T>C	NP_066007.1:n.*2239T>C
NM_181882.2:c.2034T>C , LRG_265t2:c.2034T>C	NP_870998.2:p.Val678=
XM_011527171.1:c.2034T>C	XP_011525473.1:p.Val678=
XM_011527171.2:c.2034T>C	XP_011525473.1:p.Val678=
XM_017027046.1:c.1932T>C	XP_016882535.1:p.Val644=
XM_017027047.1:c.1932T>C	XP_016882536.1:p.Val644=
NM_181882.3:c.2034T>C MANE Select	NP_870998.2:p.Val678=