Canonical Allele Identifier: CA405893984

Gene: PRX

Linked Data

• COSMIC: COSM6017509
• MyVariant Identifiers: chr19:g.40900877C>T (hg19) ; chr19:g.40394970C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.40394970C>T , CM000681.2:g.40394970C>T	GRCh38
NC_000019.9:g.40900877C>T , CM000681.1:g.40900877C>T	GRCh37
NC_000019.8:g.45592717C>T	NCBI36
NG_007979.1:g.23395G>A , LRG_265:g.23395G>A
NG_051224.1:g.252G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324001.8:c.3382G>A MANE Select	ENSP00000326018.6:p.Val1128Met
ENST00000673881.1:c.2965G>A	ENSP00000501070.1:p.Val989Met
ENST00000674005.2:c.3667G>A	ENSP00000501261.1:p.Val1223Met
ENST00000674773.1:c.2965G>A	ENSP00000502579.1:p.Val989Met
ENST00000675517.1:c.3257G>A
ENST00000676076.1:c.3243G>A
ENST00000676260.1:c.3344G>A
ENST00000676316.1:c.3269G>A
ENST00000291825.11:c.*3587G>A	ENSP00000291825.6:n.*3587G>A
ENST00000324001.7:c.3382G>A	ENSP00000326018.6:p.Val1128Met
NM_020956.2:c.*3587G>A , LRG_265t1:c.*3587G>A	NP_066007.1:n.*3587G>A
NM_181882.2:c.3382G>A , LRG_265t2:c.3382G>A	NP_870998.2:p.Val1128Met
XM_011527171.1:c.3382G>A	XP_011525473.1:p.Val1128Met
XM_011527171.2:c.3382G>A	XP_011525473.1:p.Val1128Met
XM_017027046.1:c.3280G>A	XP_016882535.1:p.Val1094Met
XM_017027047.1:c.3280G>A	XP_016882536.1:p.Val1094Met
NM_181882.3:c.3382G>A MANE Select	NP_870998.2:p.Val1128Met