Canonical Allele Identifier: CA353671104

Gene: PROS1

Linked Data

• COSMIC: COSM5690673
• MyVariant Identifiers: chr3:g.93595915G>A (hg19) ; chr3:g.93877071G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877071G>A , CM000665.2:g.93877071G>A	GRCh38
NC_000003.11:g.93595915G>A , CM000665.1:g.93595915G>A	GRCh37
NC_000003.10:g.95078605G>A	NCBI36
NG_009813.1:g.102020C>T , LRG_572:g.102020C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1765C>T	ENSP00000330021.7:p.Pro589Ser
ENST00000394236.9:c.1765C>T MANE Select	ENSP00000377783.3:p.Pro589Ser
ENST00000407433.6:c.1720C>T	ENSP00000385794.2:p.Pro574Ser
ENST00000647936.1:c.1644+2092C>T	ENSP00000496822.1:n.1644+2092C>T
ENST00000648381.1:n.1933C>T
ENST00000648853.1:c.1723C>T	ENSP00000497262.1:p.Pro575Ser
ENST00000649103.1:c.1864C>T	ENSP00000497962.1:n.1864C>T
ENST00000649585.1:c.708C>T	ENSP00000498163.1:n.708C>T
ENST00000650591.1:c.1861C>T	ENSP00000497376.1:p.Pro621Ser
ENST00000394236.7:c.1765C>T	ENSP00000377783.3:p.Pro589Ser
ENST00000407433.5:c.1372C>T	ENSP00000385794.1:p.Pro458Ser
NM_000313.3:c.1765C>T , LRG_572t1:c.1765C>T	NP_000304.2:p.Pro589Ser
NM_001314077.1:c.1861C>T , LRG_572t2:c.1861C>T	NP_001301006.1:p.Pro621Ser
NM_000313.4:c.1765C>T MANE Select	NP_000304.2:p.Pro589Ser
NM_001314077.2:c.1861C>T	NP_001301006.1:p.Pro621Ser