Canonical Allele Identifier: CA434461645

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93619661T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900817T>G , CM000665.2:g.93900817T>G	GRCh38
NC_000003.11:g.93619661T>G , CM000665.1:g.93619661T>G	GRCh37
NC_000003.10:g.95102351T>G	NCBI36
NG_009813.1:g.78274A>C , LRG_572:g.78274A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.714A>C	ENSP00000330021.7:p.Ser238=
ENST00000394236.9:c.714A>C MANE Select	ENSP00000377783.3:p.Ser238=
ENST00000407433.6:c.669A>C	ENSP00000385794.2:p.Ser223=
ENST00000647936.1:c.714A>C	ENSP00000496822.1:p.Ser238=
ENST00000648381.1:n.882A>C
ENST00000648853.1:c.672A>C	ENSP00000497262.1:p.Ser224=
ENST00000649103.1:c.813A>C	ENSP00000497962.1:n.813A>C
ENST00000650591.1:c.810A>C	ENSP00000497376.1:p.Ser270=
ENST00000394236.7:c.714A>C	ENSP00000377783.3:p.Ser238=
ENST00000407433.5:c.321A>C	ENSP00000385794.1:p.Ser107=
NM_000313.3:c.714A>C , LRG_572t1:c.714A>C	NP_000304.2:p.Ser238=
NM_001314077.1:c.810A>C , LRG_572t2:c.810A>C	NP_001301006.1:p.Ser270=
NM_000313.4:c.714A>C MANE Select	NP_000304.2:p.Ser238=
NM_001314077.2:c.810A>C	NP_001301006.1:p.Ser270=