Canonical Allele Identifier: CA353674690

Gene: PROS1

Linked Data

• dbSNP Id: rs1709035631
• MyVariant Identifiers: chr3:g.93646225C>T (hg19) ; chr3:g.93927381C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927381C>T , CM000665.2:g.93927381C>T	GRCh38
NC_000003.11:g.93646225C>T , CM000665.1:g.93646225C>T	GRCh37
NC_000003.10:g.95128915C>T	NCBI36
NG_009813.1:g.51710G>A , LRG_572:g.51710G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.103G>A	ENSP00000330021.7:p.Val35Ile
ENST00000394236.9:c.103G>A MANE Select	ENSP00000377783.3:p.Val35Ile
ENST00000407433.6:c.103G>A	ENSP00000385794.2:p.Val35Ile
ENST00000472684.2:c.-291G>A	ENSP00000419616.2:n.-291G>A
ENST00000647936.1:c.103G>A	ENSP00000496822.1:p.Val35Ile
ENST00000648381.1:n.271G>A
ENST00000648853.1:c.61G>A	ENSP00000497262.1:p.Val21Ile
ENST00000649103.1:c.82G>A	ENSP00000497962.1:p.Val28Ile
ENST00000650591.1:c.199G>A	ENSP00000497376.1:p.Val67Ile
ENST00000348974.4:c.199G>A	ENSP00000330021.6:p.Val67Ile
ENST00000394236.7:c.103G>A	ENSP00000377783.3:p.Val35Ile
ENST00000407433.5:c.-291G>A	ENSP00000385794.1:n.-291G>A
ENST00000472684.1:c.-291G>A	ENSP00000419616.1:n.-291G>A
NM_000313.3:c.103G>A , LRG_572t1:c.103G>A	NP_000304.2:p.Val35Ile
NM_001314077.1:c.199G>A , LRG_572t2:c.199G>A	NP_001301006.1:p.Val67Ile
NM_000313.4:c.103G>A MANE Select	NP_000304.2:p.Val35Ile
NM_001314077.2:c.199G>A	NP_001301006.1:p.Val67Ile