Canonical Allele Identifier: CA434459872

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93611903A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893059A>G , CM000665.2:g.93893059A>G	GRCh38
NC_000003.11:g.93611903A>G , CM000665.1:g.93611903A>G	GRCh37
NC_000003.10:g.95094593A>G	NCBI36
NG_009813.1:g.86032T>C , LRG_572:g.86032T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1029T>C	ENSP00000330021.7:p.Ser343=
ENST00000394236.9:c.1029T>C MANE Select	ENSP00000377783.3:p.Ser343=
ENST00000407433.6:c.984T>C	ENSP00000385794.2:p.Ser328=
ENST00000647936.1:c.1029T>C	ENSP00000496822.1:p.Ser343=
ENST00000648381.1:n.1197T>C
ENST00000648853.1:c.987T>C	ENSP00000497262.1:p.Ser329=
ENST00000649103.1:c.1128T>C	ENSP00000497962.1:n.1128T>C
ENST00000650591.1:c.1125T>C	ENSP00000497376.1:p.Ser375=
ENST00000394236.7:c.1029T>C	ENSP00000377783.3:p.Ser343=
ENST00000407433.5:c.636T>C	ENSP00000385794.1:p.Ser212=
NM_000313.3:c.1029T>C , LRG_572t1:c.1029T>C	NP_000304.2:p.Ser343=
NM_001314077.1:c.1125T>C , LRG_572t2:c.1125T>C	NP_001301006.1:p.Ser375=
NM_000313.4:c.1029T>C MANE Select	NP_000304.2:p.Ser343=
NM_001314077.2:c.1125T>C	NP_001301006.1:p.Ser375=