Canonical Allele Identifier: CA9444152

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396373G>C , CM000681.2:g.40396373G>C	GRCh38
NC_000019.9:g.40902280G>C , CM000681.1:g.40902280G>C	GRCh37
NC_000019.8:g.45594120G>C	NCBI36
NG_007979.1:g.21992C>G , LRG_265:g.21992C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.1979C>G MANE Select	NP_870998.2:p.Pro660Arg
ENST00000324001.8:c.1979C>G MANE Select	ENSP00000326018.6:p.Pro660Arg
NM_020956.2:c.*2184C>G , LRG_265t1:c.*2184C>G	NP_066007.1:n.*2184C>G
NM_181882.2:c.1979C>G , LRG_265t2:c.1979C>G	NP_870998.2:p.Pro660Arg
ENST00000291825.11:c.*2184C>G	ENSP00000291825.6:n.*2184C>G
ENST00000324001.7:c.1979C>G	ENSP00000326018.6:p.Pro660Arg
ENST00000673881.1:c.1562C>G	ENSP00000501070.1:p.Pro521Arg
ENST00000674005.2:c.2264C>G	ENSP00000501261.1:p.Pro755Arg
ENST00000674773.1:c.1562C>G	ENSP00000502579.1:p.Pro521Arg
ENST00000675517.1:c.1854C>G
ENST00000676076.1:c.1840C>G
ENST00000676260.1:c.1941C>G
ENST00000676316.1:c.1866C>G
XM_011527171.1:c.1979C>G	XP_011525473.1:p.Pro660Arg
XM_011527171.2:c.1979C>G	XP_011525473.1:p.Pro660Arg
XM_017027046.1:c.1877C>G	XP_016882535.1:p.Pro626Arg
XM_017027047.1:c.1877C>G	XP_016882536.1:p.Pro626Arg