Canonical Allele Identifier: CA405896713

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40902027C>G (hg19) ; chr19:g.40396120C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396120C>G , CM000681.2:g.40396120C>G	GRCh38
NC_000019.9:g.40902027C>G , CM000681.1:g.40902027C>G	GRCh37
NC_000019.8:g.45593867C>G	NCBI36
NG_007979.1:g.22245G>C , LRG_265:g.22245G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2232G>C MANE Select	ENSP00000326018.6:p.Glu744Asp
ENST00000673881.1:c.1815G>C	ENSP00000501070.1:p.Glu605Asp
ENST00000674005.2:c.2517G>C	ENSP00000501261.1:p.Glu839Asp
ENST00000674773.1:c.1815G>C	ENSP00000502579.1:p.Glu605Asp
ENST00000675517.1:c.2107G>C
ENST00000676076.1:c.2093G>C
ENST00000676260.1:c.2194G>C
ENST00000676316.1:c.2119G>C
ENST00000291825.11:c.*2437G>C	ENSP00000291825.6:n.*2437G>C
ENST00000324001.7:c.2232G>C	ENSP00000326018.6:p.Glu744Asp
NM_020956.2:c.*2437G>C , LRG_265t1:c.*2437G>C	NP_066007.1:n.*2437G>C
NM_181882.2:c.2232G>C , LRG_265t2:c.2232G>C	NP_870998.2:p.Glu744Asp
XM_011527171.1:c.2232G>C	XP_011525473.1:p.Glu744Asp
XM_011527171.2:c.2232G>C	XP_011525473.1:p.Glu744Asp
XM_017027046.1:c.2130G>C	XP_016882535.1:p.Glu710Asp
XM_017027047.1:c.2130G>C	XP_016882536.1:p.Glu710Asp
NM_181882.3:c.2232G>C MANE Select	NP_870998.2:p.Glu744Asp