Canonical Allele Identifier: CA405897066

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40902187A>C (hg19) ; chr19:g.40396280A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396280A>C , CM000681.2:g.40396280A>C	GRCh38
NC_000019.9:g.40902187A>C , CM000681.1:g.40902187A>C	GRCh37
NC_000019.8:g.45594027A>C	NCBI36
NG_007979.1:g.22085T>G , LRG_265:g.22085T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2072T>G MANE Select	ENSP00000326018.6:p.Met691Arg
ENST00000673881.1:c.1655T>G	ENSP00000501070.1:p.Met552Arg
ENST00000674005.2:c.2357T>G	ENSP00000501261.1:p.Met786Arg
ENST00000674773.1:c.1655T>G	ENSP00000502579.1:p.Met552Arg
ENST00000675517.1:c.1947T>G
ENST00000676076.1:c.1933T>G
ENST00000676260.1:c.2034T>G
ENST00000676316.1:c.1959T>G
ENST00000291825.11:c.*2277T>G	ENSP00000291825.6:n.*2277T>G
ENST00000324001.7:c.2072T>G	ENSP00000326018.6:p.Met691Arg
NM_020956.2:c.*2277T>G , LRG_265t1:c.*2277T>G	NP_066007.1:n.*2277T>G
NM_181882.2:c.2072T>G , LRG_265t2:c.2072T>G	NP_870998.2:p.Met691Arg
XM_011527171.1:c.2072T>G	XP_011525473.1:p.Met691Arg
XM_011527171.2:c.2072T>G	XP_011525473.1:p.Met691Arg
XM_017027046.1:c.1970T>G	XP_016882535.1:p.Met657Arg
XM_017027047.1:c.1970T>G	XP_016882536.1:p.Met657Arg
NM_181882.3:c.2072T>G MANE Select	NP_870998.2:p.Met691Arg