Canonical Allele Identifier: CA434460862

Gene: PROS1

Linked Data

• gnomAD v4: 3-93896656-T-C
• MyVariant Identifiers: chr3:g.93615500T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896656T>C , CM000665.2:g.93896656T>C	GRCh38
NC_000003.11:g.93615500T>C , CM000665.1:g.93615500T>C	GRCh37
NC_000003.10:g.95098190T>C	NCBI36
NG_009813.1:g.82435A>G , LRG_572:g.82435A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.885A>G	ENSP00000330021.7:p.Thr295=
ENST00000394236.9:c.885A>G MANE Select	ENSP00000377783.3:p.Thr295=
ENST00000407433.6:c.840A>G	ENSP00000385794.2:p.Thr280=
ENST00000647936.1:c.885A>G	ENSP00000496822.1:p.Thr295=
ENST00000648381.1:n.1053A>G
ENST00000648853.1:c.843A>G	ENSP00000497262.1:p.Thr281=
ENST00000649103.1:c.984A>G	ENSP00000497962.1:n.984A>G
ENST00000650591.1:c.981A>G	ENSP00000497376.1:p.Thr327=
ENST00000394236.7:c.885A>G	ENSP00000377783.3:p.Thr295=
ENST00000407433.5:c.492A>G	ENSP00000385794.1:p.Thr164=
NM_000313.3:c.885A>G , LRG_572t1:c.885A>G	NP_000304.2:p.Thr295=
NM_001314077.1:c.981A>G , LRG_572t2:c.981A>G	NP_001301006.1:p.Thr327=
NM_000313.4:c.885A>G MANE Select	NP_000304.2:p.Thr295=
NM_001314077.2:c.981A>G	NP_001301006.1:p.Thr327=