Canonical Allele Identifier: CA434464442

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598091A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879247A>G , CM000665.2:g.93879247A>G	GRCh38
NC_000003.11:g.93598091A>G , CM000665.1:g.93598091A>G	GRCh37
NC_000003.10:g.95080781A>G	NCBI36
NG_009813.1:g.99844T>C , LRG_572:g.99844T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1560T>C	ENSP00000330021.7:p.Thr520=
ENST00000394236.9:c.1560T>C MANE Select	ENSP00000377783.3:p.Thr520=
ENST00000407433.6:c.1515T>C	ENSP00000385794.2:p.Thr505=
ENST00000647936.1:c.1560T>C	ENSP00000496822.1:p.Thr520=
ENST00000648381.1:n.1728T>C
ENST00000648853.1:c.1518T>C	ENSP00000497262.1:p.Thr506=
ENST00000649103.1:c.1659T>C	ENSP00000497962.1:n.1659T>C
ENST00000649585.1:c.503T>C	ENSP00000498163.1:n.503T>C
ENST00000650591.1:c.1656T>C	ENSP00000497376.1:p.Thr552=
ENST00000394236.7:c.1560T>C	ENSP00000377783.3:p.Thr520=
ENST00000407433.5:c.1167T>C	ENSP00000385794.1:p.Thr389=
NM_000313.3:c.1560T>C , LRG_572t1:c.1560T>C	NP_000304.2:p.Thr520=
NM_001314077.1:c.1656T>C , LRG_572t2:c.1656T>C	NP_001301006.1:p.Thr552=
NM_000313.4:c.1560T>C MANE Select	NP_000304.2:p.Thr520=
NM_001314077.2:c.1656T>C	NP_001301006.1:p.Thr552=