Canonical Allele Identifier: CA353671997

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598090C>A (hg19) ; chr3:g.93879246C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1561G>T	ENSP00000330021.7:p.Gly521Cys
ENST00000394236.9:c.1561G>T MANE Select	ENSP00000377783.3:p.Gly521Cys
ENST00000407433.6:c.1516G>T	ENSP00000385794.2:p.Gly506Cys
ENST00000647936.1:c.1561G>T	ENSP00000496822.1:p.Gly521Cys
ENST00000648381.1:n.1729G>T
ENST00000648853.1:c.1519G>T	ENSP00000497262.1:p.Gly507Cys
ENST00000649103.1:c.1660G>T	ENSP00000497962.1:n.1660G>T
ENST00000649585.1:c.504G>T	ENSP00000498163.1:n.504G>T
ENST00000650591.1:c.1657G>T	ENSP00000497376.1:p.Gly553Cys
ENST00000394236.7:c.1561G>T	ENSP00000377783.3:p.Gly521Cys
ENST00000407433.5:c.1168G>T	ENSP00000385794.1:p.Gly390Cys
NM_000313.3:c.1561G>T , LRG_572t1:c.1561G>T	NP_000304.2:p.Gly521Cys
NM_001314077.1:c.1657G>T , LRG_572t2:c.1657G>T	NP_001301006.1:p.Gly553Cys
NM_000313.4:c.1561G>T MANE Select	NP_000304.2:p.Gly521Cys
NM_001314077.2:c.1657G>T	NP_001301006.1:p.Gly553Cys