Canonical Allele Identifier: CA353669572

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593144T>A (hg19) ; chr3:g.93874300T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874300T>A , CM000665.2:g.93874300T>A	GRCh38
NC_000003.11:g.93593144T>A , CM000665.1:g.93593144T>A	GRCh37
NC_000003.10:g.95075834T>A	NCBI36
NG_009813.1:g.104791A>T , LRG_572:g.104791A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1976A>T	ENSP00000330021.7:p.Asn659Ile
ENST00000394236.9:c.1976A>T MANE Select	ENSP00000377783.3:p.Asn659Ile
ENST00000407433.6:c.1931A>T	ENSP00000385794.2:p.Asn644Ile
ENST00000647936.1:c.*79A>T	ENSP00000496822.1:n.*79A>T
ENST00000648381.1:n.2144A>T
ENST00000648853.1:c.1934A>T	ENSP00000497262.1:p.Asn645Ile
ENST00000650591.1:c.2072A>T	ENSP00000497376.1:p.Asn691Ile
ENST00000394236.7:c.1976A>T	ENSP00000377783.3:p.Asn659Ile
ENST00000407433.5:c.1583A>T	ENSP00000385794.1:p.Asn528Ile
NM_000313.3:c.1976A>T , LRG_572t1:c.1976A>T	NP_000304.2:p.Asn659Ile
NM_001314077.1:c.2072A>T , LRG_572t2:c.2072A>T	NP_001301006.1:p.Asn691Ile
NM_000313.4:c.1976A>T MANE Select	NP_000304.2:p.Asn659Ile
NM_001314077.2:c.2072A>T	NP_001301006.1:p.Asn691Ile