Canonical Allele Identifier: CA353671004

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93595889A>T (hg19) ; chr3:g.93877045A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877045A>T , CM000665.2:g.93877045A>T	GRCh38
NC_000003.11:g.93595889A>T , CM000665.1:g.93595889A>T	GRCh37
NC_000003.10:g.95078579A>T	NCBI36
NG_009813.1:g.102046T>A , LRG_572:g.102046T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1791T>A	ENSP00000330021.7:p.His597Gln
ENST00000394236.9:c.1791T>A MANE Select	ENSP00000377783.3:p.His597Gln
ENST00000407433.6:c.1746T>A	ENSP00000385794.2:p.His582Gln
ENST00000647936.1:c.1644+2118T>A	ENSP00000496822.1:n.1644+2118T>A
ENST00000648381.1:n.1959T>A
ENST00000648853.1:c.1749T>A	ENSP00000497262.1:p.His583Gln
ENST00000649585.1:c.734T>A	ENSP00000498163.1:n.734T>A
ENST00000650591.1:c.1887T>A	ENSP00000497376.1:p.His629Gln
ENST00000394236.7:c.1791T>A	ENSP00000377783.3:p.His597Gln
ENST00000407433.5:c.1398T>A	ENSP00000385794.1:p.His466Gln
NM_000313.3:c.1791T>A , LRG_572t1:c.1791T>A	NP_000304.2:p.His597Gln
NM_001314077.1:c.1887T>A , LRG_572t2:c.1887T>A	NP_001301006.1:p.His629Gln
NM_000313.4:c.1791T>A MANE Select	NP_000304.2:p.His597Gln
NM_001314077.2:c.1887T>A	NP_001301006.1:p.His629Gln