Canonical Allele Identifier: CA353671458

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93596011T>A (hg19) ; chr3:g.93877167T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877167T>A , CM000665.2:g.93877167T>A	GRCh38
NC_000003.11:g.93596011T>A , CM000665.1:g.93596011T>A	GRCh37
NC_000003.10:g.95078701T>A	NCBI36
NG_009813.1:g.101924A>T , LRG_572:g.101924A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1669A>T	ENSP00000330021.7:p.Thr557Ser
ENST00000394236.9:c.1669A>T MANE Select	ENSP00000377783.3:p.Thr557Ser
ENST00000407433.6:c.1624A>T	ENSP00000385794.2:p.Thr542Ser
ENST00000647936.1:c.1644+1996A>T	ENSP00000496822.1:n.1644+1996A>T
ENST00000648381.1:n.1837A>T
ENST00000648853.1:c.1627A>T	ENSP00000497262.1:p.Thr543Ser
ENST00000649103.1:c.1768A>T	ENSP00000497962.1:n.1768A>T
ENST00000649585.1:c.612A>T	ENSP00000498163.1:n.612A>T
ENST00000650591.1:c.1765A>T	ENSP00000497376.1:p.Thr589Ser
ENST00000394236.7:c.1669A>T	ENSP00000377783.3:p.Thr557Ser
ENST00000407433.5:c.1276A>T	ENSP00000385794.1:p.Thr426Ser
NM_000313.3:c.1669A>T , LRG_572t1:c.1669A>T	NP_000304.2:p.Thr557Ser
NM_001314077.1:c.1765A>T , LRG_572t2:c.1765A>T	NP_001301006.1:p.Thr589Ser
NM_000313.4:c.1669A>T MANE Select	NP_000304.2:p.Thr557Ser
NM_001314077.2:c.1765A>T	NP_001301006.1:p.Thr589Ser