Canonical Allele Identifier: CA353672166

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598138C>A (hg19) ; chr3:g.93879294C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879294C>A , CM000665.2:g.93879294C>A	GRCh38
NC_000003.11:g.93598138C>A , CM000665.1:g.93598138C>A	GRCh37
NC_000003.10:g.95080828C>A	NCBI36
NG_009813.1:g.99797G>T , LRG_572:g.99797G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1513G>T	ENSP00000330021.7:p.Gly505Cys
ENST00000394236.9:c.1513G>T MANE Select	ENSP00000377783.3:p.Gly505Cys
ENST00000407433.6:c.1468G>T	ENSP00000385794.2:p.Gly490Cys
ENST00000647936.1:c.1513G>T	ENSP00000496822.1:p.Gly505Cys
ENST00000648381.1:n.1681G>T
ENST00000648853.1:c.1471G>T	ENSP00000497262.1:p.Gly491Cys
ENST00000649103.1:c.1612G>T	ENSP00000497962.1:n.1612G>T
ENST00000649585.1:c.456G>T	ENSP00000498163.1:n.456G>T
ENST00000650591.1:c.1609G>T	ENSP00000497376.1:p.Gly537Cys
ENST00000394236.7:c.1513G>T	ENSP00000377783.3:p.Gly505Cys
ENST00000407433.5:c.1120G>T	ENSP00000385794.1:p.Gly374Cys
NM_000313.3:c.1513G>T , LRG_572t1:c.1513G>T	NP_000304.2:p.Gly505Cys
NM_001314077.1:c.1609G>T , LRG_572t2:c.1609G>T	NP_001301006.1:p.Gly537Cys
NM_000313.4:c.1513G>T MANE Select	NP_000304.2:p.Gly505Cys
NM_001314077.2:c.1609G>T	NP_001301006.1:p.Gly537Cys