Canonical Allele Identifier: CA434460891

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615524C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896680C>G , CM000665.2:g.93896680C>G	GRCh38
NC_000003.11:g.93615524C>G , CM000665.1:g.93615524C>G	GRCh37
NC_000003.10:g.95098214C>G	NCBI36
NG_009813.1:g.82411G>C , LRG_572:g.82411G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.861G>C	ENSP00000330021.7:p.Val287=
ENST00000394236.9:c.861G>C MANE Select	ENSP00000377783.3:p.Val287=
ENST00000407433.6:c.816G>C	ENSP00000385794.2:p.Val272=
ENST00000647936.1:c.861G>C	ENSP00000496822.1:p.Val287=
ENST00000648381.1:n.1029G>C
ENST00000648853.1:c.819G>C	ENSP00000497262.1:p.Val273=
ENST00000649103.1:c.960G>C	ENSP00000497962.1:n.960G>C
ENST00000650591.1:c.957G>C	ENSP00000497376.1:p.Val319=
ENST00000394236.7:c.861G>C	ENSP00000377783.3:p.Val287=
ENST00000407433.5:c.468G>C	ENSP00000385794.1:p.Val156=
NM_000313.3:c.861G>C , LRG_572t1:c.861G>C	NP_000304.2:p.Val287=
NM_001314077.1:c.957G>C , LRG_572t2:c.957G>C	NP_001301006.1:p.Val319=
NM_000313.4:c.861G>C MANE Select	NP_000304.2:p.Val287=
NM_001314077.2:c.957G>C	NP_001301006.1:p.Val319=