Canonical Allele Identifier: CA434463043

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93595841T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93876997T>C , CM000665.2:g.93876997T>C	GRCh38
NC_000003.11:g.93595841T>C , CM000665.1:g.93595841T>C	GRCh37
NC_000003.10:g.95078531T>C	NCBI36
NG_009813.1:g.102094A>G , LRG_572:g.102094A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1839A>G	ENSP00000330021.7:p.Ala613=
ENST00000394236.9:c.1839A>G MANE Select	ENSP00000377783.3:p.Ala613=
ENST00000407433.6:c.1794A>G	ENSP00000385794.2:p.Ala598=
ENST00000647936.1:c.1644+2166A>G	ENSP00000496822.1:n.1644+2166A>G
ENST00000648381.1:n.2007A>G
ENST00000648853.1:c.1797A>G	ENSP00000497262.1:p.Ala599=
ENST00000650591.1:c.1935A>G	ENSP00000497376.1:p.Ala645=
ENST00000394236.7:c.1839A>G	ENSP00000377783.3:p.Ala613=
ENST00000407433.5:c.1446A>G	ENSP00000385794.1:p.Ala482=
NM_000313.3:c.1839A>G , LRG_572t1:c.1839A>G	NP_000304.2:p.Ala613=
NM_001314077.1:c.1935A>G , LRG_572t2:c.1935A>G	NP_001301006.1:p.Ala645=
NM_000313.4:c.1839A>G MANE Select	NP_000304.2:p.Ala613=
NM_001314077.2:c.1935A>G	NP_001301006.1:p.Ala645=