Canonical Allele Identifier: CA353673157

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93619690G>T (hg19) ; chr3:g.93900846G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900846G>T , CM000665.2:g.93900846G>T	GRCh38
NC_000003.11:g.93619690G>T , CM000665.1:g.93619690G>T	GRCh37
NC_000003.10:g.95102380G>T	NCBI36
NG_009813.1:g.78245C>A , LRG_572:g.78245C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.685C>A	ENSP00000330021.7:p.Pro229Thr
ENST00000394236.9:c.685C>A MANE Select	ENSP00000377783.3:p.Pro229Thr
ENST00000407433.6:c.640C>A	ENSP00000385794.2:p.Pro214Thr
ENST00000647936.1:c.685C>A	ENSP00000496822.1:p.Pro229Thr
ENST00000648381.1:n.853C>A
ENST00000648853.1:c.643C>A	ENSP00000497262.1:p.Pro215Thr
ENST00000649103.1:c.784C>A	ENSP00000497962.1:n.784C>A
ENST00000650591.1:c.781C>A	ENSP00000497376.1:p.Pro261Thr
ENST00000394236.7:c.685C>A	ENSP00000377783.3:p.Pro229Thr
ENST00000407433.5:c.292C>A	ENSP00000385794.1:p.Pro98Thr
NM_000313.3:c.685C>A , LRG_572t1:c.685C>A	NP_000304.2:p.Pro229Thr
NM_001314077.1:c.781C>A , LRG_572t2:c.781C>A	NP_001301006.1:p.Pro261Thr
NM_000313.4:c.685C>A MANE Select	NP_000304.2:p.Pro229Thr
NM_001314077.2:c.781C>A	NP_001301006.1:p.Pro261Thr