Canonical Allele Identifier: CA233399

Gene: PROS1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898570C>T , CM000665.2:g.93898570C>T	GRCh38
NC_000003.11:g.93617414C>T , CM000665.1:g.93617414C>T	GRCh37
NC_000003.10:g.95100104C>T	NCBI36
NG_009813.1:g.80521G>A , LRG_572:g.80521G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.728-1G>A	ENSP00000330021.7:n.728-1G>A
ENST00000394236.9:c.728-1G>A MANE Select	ENSP00000377783.3:n.728-1G>A
ENST00000407433.6:c.683-1G>A	ENSP00000385794.2:n.683-1G>A
ENST00000647936.1:c.728-1G>A	ENSP00000496822.1:n.728-1G>A
ENST00000648381.1:n.896-1G>A
ENST00000648853.1:c.686-1G>A	ENSP00000497262.1:n.686-1G>A
ENST00000649103.1:c.827-1G>A	ENSP00000497962.1:n.827-1G>A
ENST00000650591.1:c.824-1G>A	ENSP00000497376.1:n.824-1G>A
ENST00000394236.7:c.728-1G>A	ENSP00000377783.3:n.728-1G>A
ENST00000407433.5:c.335-1G>A	ENSP00000385794.1:n.335-1G>A
NM_000313.3:c.728-1G>A , LRG_572t1:c.728-1G>A	NP_000304.2:n.728-1G>A
NM_001314077.1:c.824-1G>A , LRG_572t2:c.824-1G>A	NP_001301006.1:n.824-1G>A
NM_000313.4:c.728-1G>A MANE Select	NP_000304.2:n.728-1G>A
NM_001314077.2:c.824-1G>A	NP_001301006.1:n.824-1G>A