Canonical Allele Identifier: CA434462790

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593119T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874275T>G , CM000665.2:g.93874275T>G	GRCh38
NC_000003.11:g.93593119T>G , CM000665.1:g.93593119T>G	GRCh37
NC_000003.10:g.95075809T>G	NCBI36
NG_009813.1:g.104816A>C , LRG_572:g.104816A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.2001A>C	ENSP00000330021.7:p.Pro667=
ENST00000394236.9:c.2001A>C MANE Select	ENSP00000377783.3:p.Pro667=
ENST00000407433.6:c.1956A>C	ENSP00000385794.2:p.Pro652=
ENST00000647936.1:c.*104A>C	ENSP00000496822.1:n.*104A>C
ENST00000648381.1:n.2169A>C
ENST00000648853.1:c.1959A>C	ENSP00000497262.1:p.Pro653=
ENST00000650591.1:c.2097A>C	ENSP00000497376.1:p.Pro699=
ENST00000394236.7:c.2001A>C	ENSP00000377783.3:p.Pro667=
ENST00000407433.5:c.1608A>C	ENSP00000385794.1:p.Pro536=
NM_000313.3:c.2001A>C , LRG_572t1:c.2001A>C	NP_000304.2:p.Pro667=
NM_001314077.1:c.2097A>C , LRG_572t2:c.2097A>C	NP_001301006.1:p.Pro699=
NM_000313.4:c.2001A>C MANE Select	NP_000304.2:p.Pro667=
NM_001314077.2:c.2097A>C	NP_001301006.1:p.Pro699=