Canonical Allele Identifier: CA507678701

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40900902A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394995A>G , CM000681.2:g.40394995A>G	GRCh38
NC_000019.9:g.40900902A>G , CM000681.1:g.40900902A>G	GRCh37
NC_000019.8:g.45592742A>G	NCBI36
NG_007979.1:g.23370T>C , LRG_265:g.23370T>C
NG_051224.1:g.227T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3357T>C MANE Select	ENSP00000326018.6:p.Ser1119=
ENST00000673881.1:c.2940T>C	ENSP00000501070.1:p.Ser980=
ENST00000674005.2:c.3642T>C	ENSP00000501261.1:p.Ser1214=
ENST00000674773.1:c.2940T>C	ENSP00000502579.1:p.Ser980=
ENST00000675517.1:c.3232T>C
ENST00000676076.1:c.3218T>C
ENST00000676260.1:c.3319T>C
ENST00000676316.1:c.3244T>C
ENST00000291825.11:c.*3562T>C	ENSP00000291825.6:n.*3562T>C
ENST00000324001.7:c.3357T>C	ENSP00000326018.6:p.Ser1119=
NM_020956.2:c.*3562T>C , LRG_265t1:c.*3562T>C	NP_066007.1:n.*3562T>C
NM_181882.2:c.3357T>C , LRG_265t2:c.3357T>C	NP_870998.2:p.Ser1119=
XM_011527171.1:c.3357T>C	XP_011525473.1:p.Ser1119=
XM_011527171.2:c.3357T>C	XP_011525473.1:p.Ser1119=
XM_017027046.1:c.3255T>C	XP_016882535.1:p.Ser1085=
XM_017027047.1:c.3255T>C	XP_016882536.1:p.Ser1085=
NM_181882.3:c.3357T>C MANE Select	NP_870998.2:p.Ser1119=