Canonical Allele Identifier: CA405897159

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40902233G>T (hg19) ; chr19:g.40396326G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396326G>T , CM000681.2:g.40396326G>T	GRCh38
NC_000019.9:g.40902233G>T , CM000681.1:g.40902233G>T	GRCh37
NC_000019.8:g.45594073G>T	NCBI36
NG_007979.1:g.22039C>A , LRG_265:g.22039C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2026C>A MANE Select	ENSP00000326018.6:p.Pro676Thr
ENST00000673881.1:c.1609C>A	ENSP00000501070.1:p.Pro537Thr
ENST00000674005.2:c.2311C>A	ENSP00000501261.1:p.Pro771Thr
ENST00000674773.1:c.1609C>A	ENSP00000502579.1:p.Pro537Thr
ENST00000675517.1:c.1901C>A
ENST00000676076.1:c.1887C>A
ENST00000676260.1:c.1988C>A
ENST00000676316.1:c.1913C>A
ENST00000291825.11:c.*2231C>A	ENSP00000291825.6:n.*2231C>A
ENST00000324001.7:c.2026C>A	ENSP00000326018.6:p.Pro676Thr
NM_020956.2:c.*2231C>A , LRG_265t1:c.*2231C>A	NP_066007.1:n.*2231C>A
NM_181882.2:c.2026C>A , LRG_265t2:c.2026C>A	NP_870998.2:p.Pro676Thr
XM_011527171.1:c.2026C>A	XP_011525473.1:p.Pro676Thr
XM_011527171.2:c.2026C>A	XP_011525473.1:p.Pro676Thr
XM_017027046.1:c.1924C>A	XP_016882535.1:p.Pro642Thr
XM_017027047.1:c.1924C>A	XP_016882536.1:p.Pro642Thr
NM_181882.3:c.2026C>A MANE Select	NP_870998.2:p.Pro676Thr