Canonical Allele Identifier: CA353670986

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93595885C>A (hg19) ; chr3:g.93877041C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877041C>A , CM000665.2:g.93877041C>A	GRCh38
NC_000003.11:g.93595885C>A , CM000665.1:g.93595885C>A	GRCh37
NC_000003.10:g.95078575C>A	NCBI36
NG_009813.1:g.102050G>T , LRG_572:g.102050G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1795G>T	ENSP00000330021.7:p.Asp599Tyr
ENST00000394236.9:c.1795G>T MANE Select	ENSP00000377783.3:p.Asp599Tyr
ENST00000407433.6:c.1750G>T	ENSP00000385794.2:p.Asp584Tyr
ENST00000647936.1:c.1644+2122G>T	ENSP00000496822.1:n.1644+2122G>T
ENST00000648381.1:n.1963G>T
ENST00000648853.1:c.1753G>T	ENSP00000497262.1:p.Asp585Tyr
ENST00000649585.1:c.738G>T	ENSP00000498163.1:n.738G>T
ENST00000650591.1:c.1891G>T	ENSP00000497376.1:p.Asp631Tyr
ENST00000394236.7:c.1795G>T	ENSP00000377783.3:p.Asp599Tyr
ENST00000407433.5:c.1402G>T	ENSP00000385794.1:p.Asp468Tyr
NM_000313.3:c.1795G>T , LRG_572t1:c.1795G>T	NP_000304.2:p.Asp599Tyr
NM_001314077.1:c.1891G>T , LRG_572t2:c.1891G>T	NP_001301006.1:p.Asp631Tyr
NM_000313.4:c.1795G>T MANE Select	NP_000304.2:p.Asp599Tyr
NM_001314077.2:c.1891G>T	NP_001301006.1:p.Asp631Tyr