Canonical Allele Identifier: CA434459859

Gene: PROS1

Linked Data

• gnomAD v4: 3-93893056-G-T
• MyVariant Identifiers: chr3:g.93611900G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893056G>T , CM000665.2:g.93893056G>T	GRCh38
NC_000003.11:g.93611900G>T , CM000665.1:g.93611900G>T	GRCh37
NC_000003.10:g.95094590G>T	NCBI36
NG_009813.1:g.86035C>A , LRG_572:g.86035C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1032C>A	ENSP00000330021.7:p.Ile344=
ENST00000394236.9:c.1032C>A MANE Select	ENSP00000377783.3:p.Ile344=
ENST00000407433.6:c.987C>A	ENSP00000385794.2:p.Ile329=
ENST00000647936.1:c.1032C>A	ENSP00000496822.1:p.Ile344=
ENST00000648381.1:n.1200C>A
ENST00000648853.1:c.990C>A	ENSP00000497262.1:p.Ile330=
ENST00000649103.1:c.1131C>A	ENSP00000497962.1:n.1131C>A
ENST00000650591.1:c.1128C>A	ENSP00000497376.1:p.Ile376=
ENST00000394236.7:c.1032C>A	ENSP00000377783.3:p.Ile344=
ENST00000407433.5:c.639C>A	ENSP00000385794.1:p.Ile213=
NM_000313.3:c.1032C>A , LRG_572t1:c.1032C>A	NP_000304.2:p.Ile344=
NM_001314077.1:c.1128C>A , LRG_572t2:c.1128C>A	NP_001301006.1:p.Ile376=
NM_000313.4:c.1032C>A MANE Select	NP_000304.2:p.Ile344=
NM_001314077.2:c.1128C>A	NP_001301006.1:p.Ile376=