Canonical Allele Identifier: CA507679417

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40901931C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396024C>A , CM000681.2:g.40396024C>A	GRCh38
NC_000019.9:g.40901931C>A , CM000681.1:g.40901931C>A	GRCh37
NC_000019.8:g.45593771C>A	NCBI36
NG_007979.1:g.22341G>T , LRG_265:g.22341G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.2328G>T MANE Select	ENSP00000326018.6:p.Leu776=
ENST00000673881.1:c.1911G>T	ENSP00000501070.1:p.Leu637=
ENST00000674005.2:c.2613G>T	ENSP00000501261.1:p.Leu871=
ENST00000674773.1:c.1911G>T	ENSP00000502579.1:p.Leu637=
ENST00000675517.1:c.2203G>T
ENST00000676076.1:c.2189G>T
ENST00000676260.1:c.2290G>T
ENST00000676316.1:c.2215G>T
ENST00000291825.11:c.*2533G>T	ENSP00000291825.6:n.*2533G>T
ENST00000324001.7:c.2328G>T	ENSP00000326018.6:p.Leu776=
NM_020956.2:c.*2533G>T , LRG_265t1:c.*2533G>T	NP_066007.1:n.*2533G>T
NM_181882.2:c.2328G>T , LRG_265t2:c.2328G>T	NP_870998.2:p.Leu776=
XM_011527171.1:c.2328G>T	XP_011525473.1:p.Leu776=
XM_011527171.2:c.2328G>T	XP_011525473.1:p.Leu776=
XM_017027046.1:c.2226G>T	XP_016882535.1:p.Leu742=
XM_017027047.1:c.2226G>T	XP_016882536.1:p.Leu742=
NM_181882.3:c.2328G>T MANE Select	NP_870998.2:p.Leu776=