Canonical Allele Identifier: CA434462854

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593179T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874335T>G , CM000665.2:g.93874335T>G	GRCh38
NC_000003.11:g.93593179T>G , CM000665.1:g.93593179T>G	GRCh37
NC_000003.10:g.95075869T>G	NCBI36
NG_009813.1:g.104756A>C , LRG_572:g.104756A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1941A>C	ENSP00000330021.7:p.Val647=
ENST00000394236.9:c.1941A>C MANE Select	ENSP00000377783.3:p.Val647=
ENST00000407433.6:c.1896A>C	ENSP00000385794.2:p.Val632=
ENST00000647936.1:c.*44A>C	ENSP00000496822.1:n.*44A>C
ENST00000648381.1:n.2109A>C
ENST00000648853.1:c.1899A>C	ENSP00000497262.1:p.Val633=
ENST00000650591.1:c.2037A>C	ENSP00000497376.1:p.Val679=
ENST00000394236.7:c.1941A>C	ENSP00000377783.3:p.Val647=
ENST00000407433.5:c.1548A>C	ENSP00000385794.1:p.Val516=
NM_000313.3:c.1941A>C , LRG_572t1:c.1941A>C	NP_000304.2:p.Val647=
NM_001314077.1:c.2037A>C , LRG_572t2:c.2037A>C	NP_001301006.1:p.Val679=
NM_000313.4:c.1941A>C MANE Select	NP_000304.2:p.Val647=
NM_001314077.2:c.2037A>C	NP_001301006.1:p.Val679=