Canonical Allele Identifier: CA507679577

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40902237A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396330A>C , CM000681.2:g.40396330A>C	GRCh38
NC_000019.9:g.40902237A>C , CM000681.1:g.40902237A>C	GRCh37
NC_000019.8:g.45594077A>C	NCBI36
NG_007979.1:g.22035T>G , LRG_265:g.22035T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2022T>G MANE Select	ENSP00000326018.6:p.Ala674=
ENST00000673881.1:c.1605T>G	ENSP00000501070.1:p.Ala535=
ENST00000674005.2:c.2307T>G	ENSP00000501261.1:p.Ala769=
ENST00000674773.1:c.1605T>G	ENSP00000502579.1:p.Ala535=
ENST00000675517.1:c.1897T>G
ENST00000676076.1:c.1883T>G
ENST00000676260.1:c.1984T>G
ENST00000676316.1:c.1909T>G
ENST00000291825.11:c.*2227T>G	ENSP00000291825.6:n.*2227T>G
ENST00000324001.7:c.2022T>G	ENSP00000326018.6:p.Ala674=
NM_020956.2:c.*2227T>G , LRG_265t1:c.*2227T>G	NP_066007.1:n.*2227T>G
NM_181882.2:c.2022T>G , LRG_265t2:c.2022T>G	NP_870998.2:p.Ala674=
XM_011527171.1:c.2022T>G	XP_011525473.1:p.Ala674=
XM_011527171.2:c.2022T>G	XP_011525473.1:p.Ala674=
XM_017027046.1:c.1920T>G	XP_016882535.1:p.Ala640=
XM_017027047.1:c.1920T>G	XP_016882536.1:p.Ala640=
NM_181882.3:c.2022T>G MANE Select	NP_870998.2:p.Ala674=