Canonical Allele Identifier: CA434459738

Gene: PROS1

Linked Data

• dbSNP Id: rs1708455561
• MyVariant Identifiers: chr3:g.93611873T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893029T>C , CM000665.2:g.93893029T>C	GRCh38
NC_000003.11:g.93611873T>C , CM000665.1:g.93611873T>C	GRCh37
NC_000003.10:g.95094563T>C	NCBI36
NG_009813.1:g.86062A>G , LRG_572:g.86062A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1059A>G	ENSP00000330021.7:p.Ala353=
ENST00000394236.9:c.1059A>G MANE Select	ENSP00000377783.3:p.Ala353=
ENST00000407433.6:c.1014A>G	ENSP00000385794.2:p.Ala338=
ENST00000647936.1:c.1059A>G	ENSP00000496822.1:p.Ala353=
ENST00000648381.1:n.1227A>G
ENST00000648853.1:c.1017A>G	ENSP00000497262.1:p.Ala339=
ENST00000649103.1:c.1158A>G	ENSP00000497962.1:n.1158A>G
ENST00000650591.1:c.1155A>G	ENSP00000497376.1:p.Ala385=
ENST00000394236.7:c.1059A>G	ENSP00000377783.3:p.Ala353=
ENST00000407433.5:c.666A>G	ENSP00000385794.1:p.Ala222=
NM_000313.3:c.1059A>G , LRG_572t1:c.1059A>G	NP_000304.2:p.Ala353=
NM_001314077.1:c.1155A>G , LRG_572t2:c.1155A>G	NP_001301006.1:p.Ala385=
NM_000313.4:c.1059A>G MANE Select	NP_000304.2:p.Ala353=
NM_001314077.2:c.1155A>G	NP_001301006.1:p.Ala385=