Canonical Allele Identifier: CA405894162

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40900912A>C (hg19) ; chr19:g.40395005A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395005A>C , CM000681.2:g.40395005A>C	GRCh38
NC_000019.9:g.40900912A>C , CM000681.1:g.40900912A>C	GRCh37
NC_000019.8:g.45592752A>C	NCBI36
NG_007979.1:g.23360T>G , LRG_265:g.23360T>G
NG_051224.1:g.217T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3347T>G MANE Select	ENSP00000326018.6:p.Val1116Gly
ENST00000673881.1:c.2930T>G	ENSP00000501070.1:p.Val977Gly
ENST00000674005.2:c.3632T>G	ENSP00000501261.1:p.Val1211Gly
ENST00000674773.1:c.2930T>G	ENSP00000502579.1:p.Val977Gly
ENST00000675517.1:c.3222T>G
ENST00000676076.1:c.3208T>G
ENST00000676260.1:c.3309T>G
ENST00000676316.1:c.3234T>G
ENST00000291825.11:c.*3552T>G	ENSP00000291825.6:n.*3552T>G
ENST00000324001.7:c.3347T>G	ENSP00000326018.6:p.Val1116Gly
NM_020956.2:c.*3552T>G , LRG_265t1:c.*3552T>G	NP_066007.1:n.*3552T>G
NM_181882.2:c.3347T>G , LRG_265t2:c.3347T>G	NP_870998.2:p.Val1116Gly
XM_011527171.1:c.3347T>G	XP_011525473.1:p.Val1116Gly
XM_011527171.2:c.3347T>G	XP_011525473.1:p.Val1116Gly
XM_017027046.1:c.3245T>G	XP_016882535.1:p.Val1082Gly
XM_017027047.1:c.3245T>G	XP_016882536.1:p.Val1082Gly
NM_181882.3:c.3347T>G MANE Select	NP_870998.2:p.Val1116Gly