Canonical Allele Identifier: CA353669842

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593192T>G (hg19) ; chr3:g.93874348T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874348T>G , CM000665.2:g.93874348T>G	GRCh38
NC_000003.11:g.93593192T>G , CM000665.1:g.93593192T>G	GRCh37
NC_000003.10:g.95075882T>G	NCBI36
NG_009813.1:g.104743A>C , LRG_572:g.104743A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1928A>C	ENSP00000330021.7:p.Asn643Thr
ENST00000394236.9:c.1928A>C MANE Select	ENSP00000377783.3:p.Asn643Thr
ENST00000407433.6:c.1883A>C	ENSP00000385794.2:p.Asn628Thr
ENST00000647936.1:c.*31A>C	ENSP00000496822.1:n.*31A>C
ENST00000648381.1:n.2096A>C
ENST00000648853.1:c.1886A>C	ENSP00000497262.1:p.Asn629Thr
ENST00000650591.1:c.2024A>C	ENSP00000497376.1:p.Asn675Thr
ENST00000394236.7:c.1928A>C	ENSP00000377783.3:p.Asn643Thr
ENST00000407433.5:c.1535A>C	ENSP00000385794.1:p.Asn512Thr
NM_000313.3:c.1928A>C , LRG_572t1:c.1928A>C	NP_000304.2:p.Asn643Thr
NM_001314077.1:c.2024A>C , LRG_572t2:c.2024A>C	NP_001301006.1:p.Asn675Thr
NM_000313.4:c.1928A>C MANE Select	NP_000304.2:p.Asn643Thr
NM_001314077.2:c.2024A>C	NP_001301006.1:p.Asn675Thr