Canonical Allele Identifier: CA507678816

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40900928T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395021T>G , CM000681.2:g.40395021T>G	GRCh38
NC_000019.9:g.40900928T>G , CM000681.1:g.40900928T>G	GRCh37
NC_000019.8:g.45592768T>G	NCBI36
NG_007979.1:g.23344A>C , LRG_265:g.23344A>C
NG_051224.1:g.201A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3331A>C MANE Select	ENSP00000326018.6:p.Arg1111=
ENST00000673881.1:c.2914A>C	ENSP00000501070.1:p.Arg972=
ENST00000674005.2:c.3616A>C	ENSP00000501261.1:p.Arg1206=
ENST00000674773.1:c.2914A>C	ENSP00000502579.1:p.Arg972=
ENST00000675517.1:c.3206A>C
ENST00000676076.1:c.3192A>C
ENST00000676260.1:c.3293A>C
ENST00000676316.1:c.3218A>C
ENST00000291825.11:c.*3536A>C	ENSP00000291825.6:n.*3536A>C
ENST00000324001.7:c.3331A>C	ENSP00000326018.6:p.Arg1111=
NM_020956.2:c.*3536A>C , LRG_265t1:c.*3536A>C	NP_066007.1:n.*3536A>C
NM_181882.2:c.3331A>C , LRG_265t2:c.3331A>C	NP_870998.2:p.Arg1111=
XM_011527171.1:c.3331A>C	XP_011525473.1:p.Arg1111=
XM_011527171.2:c.3331A>C	XP_011525473.1:p.Arg1111=
XM_017027046.1:c.3229A>C	XP_016882535.1:p.Arg1077=
XM_017027047.1:c.3229A>C	XP_016882536.1:p.Arg1077=
NM_181882.3:c.3331A>C MANE Select	NP_870998.2:p.Arg1111=