Canonical Allele Identifier: CA434462783

Gene: PROS1

Linked Data

• gnomAD v4: 3-93927259-G-A
• MyVariant Identifiers: chr3:g.93646103G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927259G>A , CM000665.2:g.93927259G>A	GRCh38
NC_000003.11:g.93646103G>A , CM000665.1:g.93646103G>A	GRCh37
NC_000003.10:g.95128793G>A	NCBI36
NG_009813.1:g.51832C>T , LRG_572:g.51832C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.225C>T	ENSP00000330021.7:p.Asp75=
ENST00000394236.9:c.225C>T MANE Select	ENSP00000377783.3:p.Asp75=
ENST00000407433.6:c.225C>T	ENSP00000385794.2:p.Asp75=
ENST00000472684.2:c.-169C>T	ENSP00000419616.2:n.-169C>T
ENST00000647936.1:c.225C>T	ENSP00000496822.1:p.Asp75=
ENST00000648381.1:n.393C>T
ENST00000648853.1:c.183C>T	ENSP00000497262.1:p.Asp61=
ENST00000649103.1:c.204C>T	ENSP00000497962.1:p.Asp68=
ENST00000650591.1:c.321C>T	ENSP00000497376.1:p.Asp107=
ENST00000348974.4:c.321C>T	ENSP00000330021.6:p.Asp107=
ENST00000394236.7:c.225C>T	ENSP00000377783.3:p.Asp75=
ENST00000407433.5:c.-169C>T	ENSP00000385794.1:n.-169C>T
ENST00000472684.1:c.-169C>T	ENSP00000419616.1:n.-169C>T
NM_000313.3:c.225C>T , LRG_572t1:c.225C>T	NP_000304.2:p.Asp75=
NM_001314077.1:c.321C>T , LRG_572t2:c.321C>T	NP_001301006.1:p.Asp107=
NM_000313.4:c.225C>T MANE Select	NP_000304.2:p.Asp75=
NM_001314077.2:c.321C>T	NP_001301006.1:p.Asp107=