Canonical Allele Identifier: CA405896795

Gene: PRX

Linked Data

• gnomAD v4: 19-40396158-C-A
• MyVariant Identifiers: chr19:g.40902065C>A (hg19) ; chr19:g.40396158C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396158C>A , CM000681.2:g.40396158C>A	GRCh38
NC_000019.9:g.40902065C>A , CM000681.1:g.40902065C>A	GRCh37
NC_000019.8:g.45593905C>A	NCBI36
NG_007979.1:g.22207G>T , LRG_265:g.22207G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2194G>T MANE Select	ENSP00000326018.6:p.Val732Leu
ENST00000673881.1:c.1777G>T	ENSP00000501070.1:p.Val593Leu
ENST00000674005.2:c.2479G>T	ENSP00000501261.1:p.Val827Leu
ENST00000674773.1:c.1777G>T	ENSP00000502579.1:p.Val593Leu
ENST00000675517.1:c.2069G>T
ENST00000676076.1:c.2055G>T
ENST00000676260.1:c.2156G>T
ENST00000676316.1:c.2081G>T
ENST00000291825.11:c.*2399G>T	ENSP00000291825.6:n.*2399G>T
ENST00000324001.7:c.2194G>T	ENSP00000326018.6:p.Val732Leu
NM_020956.2:c.*2399G>T , LRG_265t1:c.*2399G>T	NP_066007.1:n.*2399G>T
NM_181882.2:c.2194G>T , LRG_265t2:c.2194G>T	NP_870998.2:p.Val732Leu
XM_011527171.1:c.2194G>T	XP_011525473.1:p.Val732Leu
XM_011527171.2:c.2194G>T	XP_011525473.1:p.Val732Leu
XM_017027046.1:c.2092G>T	XP_016882535.1:p.Val698Leu
XM_017027047.1:c.2092G>T	XP_016882536.1:p.Val698Leu
NM_181882.3:c.2194G>T MANE Select	NP_870998.2:p.Val732Leu