Canonical Allele Identifier: CA353674704

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646231A>T (hg19) ; chr3:g.93927387A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927387A>T , CM000665.2:g.93927387A>T	GRCh38
NC_000003.11:g.93646231A>T , CM000665.1:g.93646231A>T	GRCh37
NC_000003.10:g.95128921A>T	NCBI36
NG_009813.1:g.51704T>A , LRG_572:g.51704T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.97T>A	ENSP00000330021.7:p.Ser33Thr
ENST00000394236.9:c.97T>A MANE Select	ENSP00000377783.3:p.Ser33Thr
ENST00000407433.6:c.97T>A	ENSP00000385794.2:p.Ser33Thr
ENST00000472684.2:c.-297T>A	ENSP00000419616.2:n.-297T>A
ENST00000647936.1:c.97T>A	ENSP00000496822.1:p.Ser33Thr
ENST00000648381.1:n.265T>A
ENST00000648853.1:c.55T>A	ENSP00000497262.1:p.Ser19Thr
ENST00000649103.1:c.76T>A	ENSP00000497962.1:p.Ser26Thr
ENST00000650591.1:c.193T>A	ENSP00000497376.1:p.Ser65Thr
ENST00000348974.4:c.193T>A	ENSP00000330021.6:p.Ser65Thr
ENST00000394236.7:c.97T>A	ENSP00000377783.3:p.Ser33Thr
ENST00000407433.5:c.-297T>A	ENSP00000385794.1:n.-297T>A
ENST00000472684.1:c.-297T>A	ENSP00000419616.1:n.-297T>A
NM_000313.3:c.97T>A , LRG_572t1:c.97T>A	NP_000304.2:p.Ser33Thr
NM_001314077.1:c.193T>A , LRG_572t2:c.193T>A	NP_001301006.1:p.Ser65Thr
NM_000313.4:c.97T>A MANE Select	NP_000304.2:p.Ser33Thr
NM_001314077.2:c.193T>A	NP_001301006.1:p.Ser65Thr