Canonical Allele Identifier: CA434460864

Gene: PROS1

Linked Data

• gnomAD v4: 3-93896659-G-A
• MyVariant Identifiers: chr3:g.93615503G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896659G>A , CM000665.2:g.93896659G>A	GRCh38
NC_000003.11:g.93615503G>A , CM000665.1:g.93615503G>A	GRCh37
NC_000003.10:g.95098193G>A	NCBI36
NG_009813.1:g.82432C>T , LRG_572:g.82432C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.882C>T	ENSP00000330021.7:p.Asp294=
ENST00000394236.9:c.882C>T MANE Select	ENSP00000377783.3:p.Asp294=
ENST00000407433.6:c.837C>T	ENSP00000385794.2:p.Asp279=
ENST00000647936.1:c.882C>T	ENSP00000496822.1:p.Asp294=
ENST00000648381.1:n.1050C>T
ENST00000648853.1:c.840C>T	ENSP00000497262.1:p.Asp280=
ENST00000649103.1:c.981C>T	ENSP00000497962.1:n.981C>T
ENST00000650591.1:c.978C>T	ENSP00000497376.1:p.Asp326=
ENST00000394236.7:c.882C>T	ENSP00000377783.3:p.Asp294=
ENST00000407433.5:c.489C>T	ENSP00000385794.1:p.Asp163=
NM_000313.3:c.882C>T , LRG_572t1:c.882C>T	NP_000304.2:p.Asp294=
NM_001314077.1:c.978C>T , LRG_572t2:c.978C>T	NP_001301006.1:p.Asp326=
NM_000313.4:c.882C>T MANE Select	NP_000304.2:p.Asp294=
NM_001314077.2:c.978C>T	NP_001301006.1:p.Asp326=