Canonical Allele Identifier: CA434462772

Gene: PROS1

Linked Data

• gnomAD v4: 3-93874257-T-C
• MyVariant Identifiers: chr3:g.93593101T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874257T>C , CM000665.2:g.93874257T>C	GRCh38
NC_000003.11:g.93593101T>C , CM000665.1:g.93593101T>C	GRCh37
NC_000003.10:g.95075791T>C	NCBI36
NG_009813.1:g.104834A>G , LRG_572:g.104834A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.2019A>G	ENSP00000330021.7:p.Thr673=
ENST00000394236.9:c.2019A>G MANE Select	ENSP00000377783.3:p.Thr673=
ENST00000407433.6:c.1974A>G	ENSP00000385794.2:p.Thr658=
ENST00000647936.1:c.*122A>G	ENSP00000496822.1:n.*122A>G
ENST00000648381.1:n.2187A>G
ENST00000648853.1:c.1977A>G	ENSP00000497262.1:p.Thr659=
ENST00000650591.1:c.2115A>G	ENSP00000497376.1:p.Thr705=
ENST00000394236.7:c.2019A>G	ENSP00000377783.3:p.Thr673=
ENST00000407433.5:c.1626A>G	ENSP00000385794.1:p.Thr542=
NM_000313.3:c.2019A>G , LRG_572t1:c.2019A>G	NP_000304.2:p.Thr673=
NM_001314077.1:c.2115A>G , LRG_572t2:c.2115A>G	NP_001301006.1:p.Thr705=
NM_000313.4:c.2019A>G MANE Select	NP_000304.2:p.Thr673=
NM_001314077.2:c.2115A>G	NP_001301006.1:p.Thr705=