Canonical Allele Identifier: CA353673185

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93619701T>G (hg19) ; chr3:g.93900857T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900857T>G , CM000665.2:g.93900857T>G	GRCh38
NC_000003.11:g.93619701T>G , CM000665.1:g.93619701T>G	GRCh37
NC_000003.10:g.95102391T>G	NCBI36
NG_009813.1:g.78234A>C , LRG_572:g.78234A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.674A>C	ENSP00000330021.7:p.Glu225Ala
ENST00000394236.9:c.674A>C MANE Select	ENSP00000377783.3:p.Glu225Ala
ENST00000407433.6:c.629A>C	ENSP00000385794.2:p.Glu210Ala
ENST00000647936.1:c.674A>C	ENSP00000496822.1:p.Glu225Ala
ENST00000648381.1:n.842A>C
ENST00000648853.1:c.632A>C	ENSP00000497262.1:p.Glu211Ala
ENST00000649103.1:c.773A>C	ENSP00000497962.1:n.773A>C
ENST00000650591.1:c.770A>C	ENSP00000497376.1:p.Glu257Ala
ENST00000394236.7:c.674A>C	ENSP00000377783.3:p.Glu225Ala
ENST00000407433.5:c.281A>C	ENSP00000385794.1:p.Glu94Ala
NM_000313.3:c.674A>C , LRG_572t1:c.674A>C	NP_000304.2:p.Glu225Ala
NM_001314077.1:c.770A>C , LRG_572t2:c.770A>C	NP_001301006.1:p.Glu257Ala
NM_000313.4:c.674A>C MANE Select	NP_000304.2:p.Glu225Ala
NM_001314077.2:c.770A>C	NP_001301006.1:p.Glu257Ala