Canonical Allele Identifier: CA353673078

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93619653C>G (hg19) ; chr3:g.93900809C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900809C>G , CM000665.2:g.93900809C>G	GRCh38
NC_000003.11:g.93619653C>G , CM000665.1:g.93619653C>G	GRCh37
NC_000003.10:g.95102343C>G	NCBI36
NG_009813.1:g.78282G>C , LRG_572:g.78282G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.722G>C	ENSP00000330021.7:p.Cys241Ser
ENST00000394236.9:c.722G>C MANE Select	ENSP00000377783.3:p.Cys241Ser
ENST00000407433.6:c.677G>C	ENSP00000385794.2:p.Cys226Ser
ENST00000647936.1:c.722G>C	ENSP00000496822.1:p.Cys241Ser
ENST00000648381.1:n.890G>C
ENST00000648853.1:c.680G>C	ENSP00000497262.1:p.Cys227Ser
ENST00000649103.1:c.821G>C	ENSP00000497962.1:n.821G>C
ENST00000650591.1:c.818G>C	ENSP00000497376.1:p.Cys273Ser
ENST00000394236.7:c.722G>C	ENSP00000377783.3:p.Cys241Ser
ENST00000407433.5:c.329G>C	ENSP00000385794.1:p.Cys110Ser
NM_000313.3:c.722G>C , LRG_572t1:c.722G>C	NP_000304.2:p.Cys241Ser
NM_001314077.1:c.818G>C , LRG_572t2:c.818G>C	NP_001301006.1:p.Cys273Ser
NM_000313.4:c.722G>C MANE Select	NP_000304.2:p.Cys241Ser
NM_001314077.2:c.818G>C	NP_001301006.1:p.Cys273Ser