Canonical Allele Identifier: CA434463959

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93596006T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877162T>A , CM000665.2:g.93877162T>A	GRCh38
NC_000003.11:g.93596006T>A , CM000665.1:g.93596006T>A	GRCh37
NC_000003.10:g.95078696T>A	NCBI36
NG_009813.1:g.101929A>T , LRG_572:g.101929A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1674A>T	ENSP00000330021.7:p.Val558=
ENST00000394236.9:c.1674A>T MANE Select	ENSP00000377783.3:p.Val558=
ENST00000407433.6:c.1629A>T	ENSP00000385794.2:p.Val543=
ENST00000647936.1:c.1644+2001A>T	ENSP00000496822.1:n.1644+2001A>T
ENST00000648381.1:n.1842A>T
ENST00000648853.1:c.1632A>T	ENSP00000497262.1:p.Val544=
ENST00000649103.1:c.1773A>T	ENSP00000497962.1:n.1773A>T
ENST00000649585.1:c.617A>T	ENSP00000498163.1:n.617A>T
ENST00000650591.1:c.1770A>T	ENSP00000497376.1:p.Val590=
ENST00000394236.7:c.1674A>T	ENSP00000377783.3:p.Val558=
ENST00000407433.5:c.1281A>T	ENSP00000385794.1:p.Val427=
NM_000313.3:c.1674A>T , LRG_572t1:c.1674A>T	NP_000304.2:p.Val558=
NM_001314077.1:c.1770A>T , LRG_572t2:c.1770A>T	NP_001301006.1:p.Val590=
NM_000313.4:c.1674A>T MANE Select	NP_000304.2:p.Val558=
NM_001314077.2:c.1770A>T	NP_001301006.1:p.Val590=