Canonical Allele Identifier: CA9443966

Gene: PRX

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40395502C>G , CM000681.2:g.40395502C>G	GRCh38
NC_000019.9:g.40901409C>G , CM000681.1:g.40901409C>G	GRCh37
NC_000019.8:g.45593249C>G	NCBI36
NG_007979.1:g.22863G>C , LRG_265:g.22863G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_181882.3:c.2850G>C MANE Select	NP_870998.2:p.Gly950=
ENST00000324001.8:c.2850G>C MANE Select	ENSP00000326018.6:p.Gly950=
NM_020956.2:c.*3055G>C , LRG_265t1:c.*3055G>C	NP_066007.1:n.*3055G>C
NM_181882.2:c.2850G>C , LRG_265t2:c.2850G>C	NP_870998.2:p.Gly950=
ENST00000291825.11:c.*3055G>C	ENSP00000291825.6:n.*3055G>C
ENST00000324001.7:c.2850G>C	ENSP00000326018.6:p.Gly950=
ENST00000673881.1:c.2433G>C	ENSP00000501070.1:p.Gly811=
ENST00000674005.2:c.3135G>C	ENSP00000501261.1:p.Gly1045=
ENST00000674773.1:c.2433G>C	ENSP00000502579.1:p.Gly811=
ENST00000675517.1:c.2725G>C
ENST00000676076.1:c.2711G>C
ENST00000676260.1:c.2812G>C
ENST00000676316.1:c.2737G>C
XM_011527171.1:c.2850G>C	XP_011525473.1:p.Gly950=
XM_011527171.2:c.2850G>C	XP_011525473.1:p.Gly950=
XM_017027046.1:c.2748G>C	XP_016882535.1:p.Gly916=
XM_017027047.1:c.2748G>C	XP_016882536.1:p.Gly916=