Canonical Allele Identifier: CA353669433

Gene: PROS1

Linked Data

• dbSNP Id: rs1297012814
• gnomAD v3: 3-93874271-C-A
• gnomAD v4: 3-93874271-C-A
• MyVariant Identifiers: chr3:g.93593115C>A (hg19) ; chr3:g.93874271C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874271C>A , CM000665.2:g.93874271C>A	GRCh38
NC_000003.11:g.93593115C>A , CM000665.1:g.93593115C>A	GRCh37
NC_000003.10:g.95075805C>A	NCBI36
NG_009813.1:g.104820G>T , LRG_572:g.104820G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.2005G>T	ENSP00000330021.7:p.Val669Phe
ENST00000394236.9:c.2005G>T MANE Select	ENSP00000377783.3:p.Val669Phe
ENST00000407433.6:c.1960G>T	ENSP00000385794.2:p.Val654Phe
ENST00000647936.1:c.*108G>T	ENSP00000496822.1:n.*108G>T
ENST00000648381.1:n.2173G>T
ENST00000648853.1:c.1963G>T	ENSP00000497262.1:p.Val655Phe
ENST00000650591.1:c.2101G>T	ENSP00000497376.1:p.Val701Phe
ENST00000394236.7:c.2005G>T	ENSP00000377783.3:p.Val669Phe
ENST00000407433.5:c.1612G>T	ENSP00000385794.1:p.Val538Phe
NM_000313.3:c.2005G>T , LRG_572t1:c.2005G>T	NP_000304.2:p.Val669Phe
NM_001314077.1:c.2101G>T , LRG_572t2:c.2101G>T	NP_001301006.1:p.Val701Phe
NM_000313.4:c.2005G>T MANE Select	NP_000304.2:p.Val669Phe
NM_001314077.2:c.2101G>T	NP_001301006.1:p.Val701Phe