Canonical Allele Identifier: CA434463024

Gene: PROS1

Linked Data

• gnomAD v4: 3-93876973-G-T
• MyVariant Identifiers: chr3:g.93595817G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93876973G>T , CM000665.2:g.93876973G>T	GRCh38
NC_000003.11:g.93595817G>T , CM000665.1:g.93595817G>T	GRCh37
NC_000003.10:g.95078507G>T	NCBI36
NG_009813.1:g.102118C>A , LRG_572:g.102118C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1863C>A	ENSP00000330021.7:p.Gly621=
ENST00000394236.9:c.1863C>A MANE Select	ENSP00000377783.3:p.Gly621=
ENST00000407433.6:c.1818C>A	ENSP00000385794.2:p.Gly606=
ENST00000647936.1:c.1644+2190C>A	ENSP00000496822.1:n.1644+2190C>A
ENST00000648381.1:n.2031C>A
ENST00000648853.1:c.1821C>A	ENSP00000497262.1:p.Gly607=
ENST00000650591.1:c.1959C>A	ENSP00000497376.1:p.Gly653=
ENST00000394236.7:c.1863C>A	ENSP00000377783.3:p.Gly621=
ENST00000407433.5:c.1470C>A	ENSP00000385794.1:p.Gly490=
NM_000313.3:c.1863C>A , LRG_572t1:c.1863C>A	NP_000304.2:p.Gly621=
NM_001314077.1:c.1959C>A , LRG_572t2:c.1959C>A	NP_001301006.1:p.Gly653=
NM_000313.4:c.1863C>A MANE Select	NP_000304.2:p.Gly621=
NM_001314077.2:c.1959C>A	NP_001301006.1:p.Gly653=