Canonical Allele Identifier: CA507679571

Gene: PRX

Linked Data

• MyVariant Identifiers: chr19:g.40902231T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40396324T>A , CM000681.2:g.40396324T>A	GRCh38
NC_000019.9:g.40902231T>A , CM000681.1:g.40902231T>A	GRCh37
NC_000019.8:g.45594071T>A	NCBI36
NG_007979.1:g.22041A>T , LRG_265:g.22041A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000324001.8:c.2028A>T MANE Select	ENSP00000326018.6:p.Pro676=
ENST00000673881.1:c.1611A>T	ENSP00000501070.1:p.Pro537=
ENST00000674005.2:c.2313A>T	ENSP00000501261.1:p.Pro771=
ENST00000674773.1:c.1611A>T	ENSP00000502579.1:p.Pro537=
ENST00000675517.1:c.1903A>T
ENST00000676076.1:c.1889A>T
ENST00000676260.1:c.1990A>T
ENST00000676316.1:c.1915A>T
ENST00000291825.11:c.*2233A>T	ENSP00000291825.6:n.*2233A>T
ENST00000324001.7:c.2028A>T	ENSP00000326018.6:p.Pro676=
NM_020956.2:c.*2233A>T , LRG_265t1:c.*2233A>T	NP_066007.1:n.*2233A>T
NM_181882.2:c.2028A>T , LRG_265t2:c.2028A>T	NP_870998.2:p.Pro676=
XM_011527171.1:c.2028A>T	XP_011525473.1:p.Pro676=
XM_011527171.2:c.2028A>T	XP_011525473.1:p.Pro676=
XM_017027046.1:c.1926A>T	XP_016882535.1:p.Pro642=
XM_017027047.1:c.1926A>T	XP_016882536.1:p.Pro642=
NM_181882.3:c.2028A>T MANE Select	NP_870998.2:p.Pro676=