Canonical Allele Identifier: CA434461712

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93619769C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900925C>A , CM000665.2:g.93900925C>A	GRCh38
NC_000003.11:g.93619769C>A , CM000665.1:g.93619769C>A	GRCh37
NC_000003.10:g.95102459C>A	NCBI36
NG_009813.1:g.78166G>T , LRG_572:g.78166G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.606G>T	ENSP00000330021.7:p.Val202=
ENST00000394236.9:c.606G>T MANE Select	ENSP00000377783.3:p.Val202=
ENST00000407433.6:c.561G>T	ENSP00000385794.2:p.Val187=
ENST00000647936.1:c.606G>T	ENSP00000496822.1:p.Val202=
ENST00000648381.1:n.774G>T
ENST00000648853.1:c.564G>T	ENSP00000497262.1:p.Val188=
ENST00000649103.1:c.705G>T	ENSP00000497962.1:n.705G>T
ENST00000650591.1:c.702G>T	ENSP00000497376.1:p.Val234=
ENST00000394236.7:c.606G>T	ENSP00000377783.3:p.Val202=
ENST00000407433.5:c.213G>T	ENSP00000385794.1:p.Val71=
NM_000313.3:c.606G>T , LRG_572t1:c.606G>T	NP_000304.2:p.Val202=
NM_001314077.1:c.702G>T , LRG_572t2:c.702G>T	NP_001301006.1:p.Val234=
NM_000313.4:c.606G>T MANE Select	NP_000304.2:p.Val202=
NM_001314077.2:c.702G>T	NP_001301006.1:p.Val234=