Canonical Allele Identifier: CA353672209

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598158T>C (hg19) ; chr3:g.93879314T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879314T>C , CM000665.2:g.93879314T>C	GRCh38
NC_000003.11:g.93598158T>C , CM000665.1:g.93598158T>C	GRCh37
NC_000003.10:g.95080848T>C	NCBI36
NG_009813.1:g.99777A>G , LRG_572:g.99777A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1493A>G	ENSP00000330021.7:p.Asn498Ser
ENST00000394236.9:c.1493A>G MANE Select	ENSP00000377783.3:p.Asn498Ser
ENST00000407433.6:c.1448A>G	ENSP00000385794.2:p.Asn483Ser
ENST00000647936.1:c.1493A>G	ENSP00000496822.1:p.Asn498Ser
ENST00000648381.1:n.1661A>G
ENST00000648853.1:c.1451A>G	ENSP00000497262.1:p.Asn484Ser
ENST00000649103.1:c.1592A>G	ENSP00000497962.1:n.1592A>G
ENST00000649585.1:c.436A>G	ENSP00000498163.1:n.436A>G
ENST00000650591.1:c.1589A>G	ENSP00000497376.1:p.Asn530Ser
ENST00000394236.7:c.1493A>G	ENSP00000377783.3:p.Asn498Ser
ENST00000407433.5:c.1100A>G	ENSP00000385794.1:p.Asn367Ser
NM_000313.3:c.1493A>G , LRG_572t1:c.1493A>G	NP_000304.2:p.Asn498Ser
NM_001314077.1:c.1589A>G , LRG_572t2:c.1589A>G	NP_001301006.1:p.Asn530Ser
NM_000313.4:c.1493A>G MANE Select	NP_000304.2:p.Asn498Ser
NM_001314077.2:c.1589A>G	NP_001301006.1:p.Asn530Ser