Canonical Allele Identifier: CA405896307

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40901834G>C (hg19) ; chr19:g.40395927G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395927G>C , CM000681.2:g.40395927G>C	GRCh38
NC_000019.9:g.40901834G>C , CM000681.1:g.40901834G>C	GRCh37
NC_000019.8:g.45593674G>C	NCBI36
NG_007979.1:g.22438C>G , LRG_265:g.22438C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.2425C>G MANE Select	ENSP00000326018.6:p.Leu809Val
ENST00000673881.1:c.2008C>G	ENSP00000501070.1:p.Leu670Val
ENST00000674005.2:c.2710C>G	ENSP00000501261.1:p.Leu904Val
ENST00000674773.1:c.2008C>G	ENSP00000502579.1:p.Leu670Val
ENST00000675517.1:c.2300C>G
ENST00000676076.1:c.2286C>G
ENST00000676260.1:c.2387C>G
ENST00000676316.1:c.2312C>G
ENST00000291825.11:c.*2630C>G	ENSP00000291825.6:n.*2630C>G
ENST00000324001.7:c.2425C>G	ENSP00000326018.6:p.Leu809Val
NM_020956.2:c.*2630C>G , LRG_265t1:c.*2630C>G	NP_066007.1:n.*2630C>G
NM_181882.2:c.2425C>G , LRG_265t2:c.2425C>G	NP_870998.2:p.Leu809Val
XM_011527171.1:c.2425C>G	XP_011525473.1:p.Leu809Val
XM_011527171.2:c.2425C>G	XP_011525473.1:p.Leu809Val
XM_017027046.1:c.2323C>G	XP_016882535.1:p.Leu775Val
XM_017027047.1:c.2323C>G	XP_016882536.1:p.Leu775Val
NM_181882.3:c.2425C>G MANE Select	NP_870998.2:p.Leu809Val