Canonical Allele Identifier: CA2577828344

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896790T>C , CM000665.2:g.93896790T>C	GRCh38
NC_000003.11:g.93615634T>C , CM000665.1:g.93615634T>C	GRCh37
NC_000003.10:g.95098324T>C	NCBI36
NG_009813.1:g.82301A>G , LRG_572:g.82301A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.850-99A>G	ENSP00000330021.7:n.850-99A>G
ENST00000394236.9:c.850-99A>G MANE Select	ENSP00000377783.3:n.850-99A>G
ENST00000407433.6:c.805-99A>G	ENSP00000385794.2:n.805-99A>G
ENST00000647936.1:c.850-99A>G	ENSP00000496822.1:n.850-99A>G
ENST00000648381.1:n.1018-99A>G
ENST00000648853.1:c.808-99A>G	ENSP00000497262.1:n.808-99A>G
ENST00000649103.1:c.949-99A>G	ENSP00000497962.1:n.949-99A>G
ENST00000650591.1:c.946-99A>G	ENSP00000497376.1:n.946-99A>G
ENST00000394236.7:c.850-99A>G	ENSP00000377783.3:n.850-99A>G
ENST00000407433.5:c.457-99A>G	ENSP00000385794.1:n.457-99A>G
NM_000313.3:c.850-99A>G , LRG_572t1:c.850-99A>G	NP_000304.2:n.850-99A>G
NM_001314077.1:c.946-99A>G , LRG_572t2:c.946-99A>G	NP_001301006.1:n.946-99A>G
NM_000313.4:c.850-99A>G MANE Select	NP_000304.2:n.850-99A>G
NM_001314077.2:c.946-99A>G	NP_001301006.1:n.946-99A>G