Canonical Allele Identifier: CA507678797

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40900923T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395016T>G , CM000681.2:g.40395016T>G	GRCh38
NC_000019.9:g.40900923T>G , CM000681.1:g.40900923T>G	GRCh37
NC_000019.8:g.45592763T>G	NCBI36
NG_007979.1:g.23349A>C , LRG_265:g.23349A>C
NG_051224.1:g.206A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3336A>C MANE Select	ENSP00000326018.6:p.Ala1112=
ENST00000673881.1:c.2919A>C	ENSP00000501070.1:p.Ala973=
ENST00000674005.2:c.3621A>C	ENSP00000501261.1:p.Ala1207=
ENST00000674773.1:c.2919A>C	ENSP00000502579.1:p.Ala973=
ENST00000675517.1:c.3211A>C
ENST00000676076.1:c.3197A>C
ENST00000676260.1:c.3298A>C
ENST00000676316.1:c.3223A>C
ENST00000291825.11:c.*3541A>C	ENSP00000291825.6:n.*3541A>C
ENST00000324001.7:c.3336A>C	ENSP00000326018.6:p.Ala1112=
NM_020956.2:c.*3541A>C , LRG_265t1:c.*3541A>C	NP_066007.1:n.*3541A>C
NM_181882.2:c.3336A>C , LRG_265t2:c.3336A>C	NP_870998.2:p.Ala1112=
XM_011527171.1:c.3336A>C	XP_011525473.1:p.Ala1112=
XM_011527171.2:c.3336A>C	XP_011525473.1:p.Ala1112=
XM_017027046.1:c.3234A>C	XP_016882535.1:p.Ala1078=
XM_017027047.1:c.3234A>C	XP_016882536.1:p.Ala1078=
NM_181882.3:c.3336A>C MANE Select	NP_870998.2:p.Ala1112=