Canonical Allele Identifier: CA353671986

Gene: PROS1

Linked Data

• gnomAD v4: 3-93879246-C-T
• MyVariant Identifiers: chr3:g.93598090C>T (hg19) ; chr3:g.93879246C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879246C>T , CM000665.2:g.93879246C>T	GRCh38
NC_000003.11:g.93598090C>T , CM000665.1:g.93598090C>T	GRCh37
NC_000003.10:g.95080780C>T	NCBI36
NG_009813.1:g.99845G>A , LRG_572:g.99845G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1561G>A	ENSP00000330021.7:p.Gly521Ser
ENST00000394236.9:c.1561G>A MANE Select	ENSP00000377783.3:p.Gly521Ser
ENST00000407433.6:c.1516G>A	ENSP00000385794.2:p.Gly506Ser
ENST00000647936.1:c.1561G>A	ENSP00000496822.1:p.Gly521Ser
ENST00000648381.1:n.1729G>A
ENST00000648853.1:c.1519G>A	ENSP00000497262.1:p.Gly507Ser
ENST00000649103.1:c.1660G>A	ENSP00000497962.1:n.1660G>A
ENST00000649585.1:c.504G>A	ENSP00000498163.1:n.504G>A
ENST00000650591.1:c.1657G>A	ENSP00000497376.1:p.Gly553Ser
ENST00000394236.7:c.1561G>A	ENSP00000377783.3:p.Gly521Ser
ENST00000407433.5:c.1168G>A	ENSP00000385794.1:p.Gly390Ser
NM_000313.3:c.1561G>A , LRG_572t1:c.1561G>A	NP_000304.2:p.Gly521Ser
NM_001314077.1:c.1657G>A , LRG_572t2:c.1657G>A	NP_001301006.1:p.Gly553Ser
NM_000313.4:c.1561G>A MANE Select	NP_000304.2:p.Gly521Ser
NM_001314077.2:c.1657G>A	NP_001301006.1:p.Gly553Ser