Canonical Allele Identifier: CA353671045

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93595901T>G (hg19) ; chr3:g.93877057T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877057T>G , CM000665.2:g.93877057T>G	GRCh38
NC_000003.11:g.93595901T>G , CM000665.1:g.93595901T>G	GRCh37
NC_000003.10:g.95078591T>G	NCBI36
NG_009813.1:g.102034A>C , LRG_572:g.102034A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1779A>C	ENSP00000330021.7:p.Glu593Asp
ENST00000394236.9:c.1779A>C MANE Select	ENSP00000377783.3:p.Glu593Asp
ENST00000407433.6:c.1734A>C	ENSP00000385794.2:p.Glu578Asp
ENST00000647936.1:c.1644+2106A>C	ENSP00000496822.1:n.1644+2106A>C
ENST00000648381.1:n.1947A>C
ENST00000648853.1:c.1737A>C	ENSP00000497262.1:p.Glu579Asp
ENST00000649103.1:c.1878A>C	ENSP00000497962.1:n.1878A>C
ENST00000649585.1:c.722A>C	ENSP00000498163.1:n.722A>C
ENST00000650591.1:c.1875A>C	ENSP00000497376.1:p.Glu625Asp
ENST00000394236.7:c.1779A>C	ENSP00000377783.3:p.Glu593Asp
ENST00000407433.5:c.1386A>C	ENSP00000385794.1:p.Glu462Asp
NM_000313.3:c.1779A>C , LRG_572t1:c.1779A>C	NP_000304.2:p.Glu593Asp
NM_001314077.1:c.1875A>C , LRG_572t2:c.1875A>C	NP_001301006.1:p.Glu625Asp
NM_000313.4:c.1779A>C MANE Select	NP_000304.2:p.Glu593Asp
NM_001314077.2:c.1875A>C	NP_001301006.1:p.Glu625Asp