Canonical Allele Identifier: CA353670098

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593223T>C (hg19) ; chr3:g.93874379T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874379T>C , CM000665.2:g.93874379T>C	GRCh38
NC_000003.11:g.93593223T>C , CM000665.1:g.93593223T>C	GRCh37
NC_000003.10:g.95075913T>C	NCBI36
NG_009813.1:g.104712A>G , LRG_572:g.104712A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1897A>G	ENSP00000330021.7:p.Asn633Asp
ENST00000394236.9:c.1897A>G MANE Select	ENSP00000377783.3:p.Asn633Asp
ENST00000407433.6:c.1852A>G	ENSP00000385794.2:p.Asn618Asp
ENST00000647936.1:c.1671A>G	ENSP00000496822.1:p.Ter557Trp
ENST00000648381.1:n.2065A>G
ENST00000648853.1:c.1855A>G	ENSP00000497262.1:p.Asn619Asp
ENST00000650591.1:c.1993A>G	ENSP00000497376.1:p.Asn665Asp
ENST00000394236.7:c.1897A>G	ENSP00000377783.3:p.Asn633Asp
ENST00000407433.5:c.1504A>G	ENSP00000385794.1:p.Asn502Asp
NM_000313.3:c.1897A>G , LRG_572t1:c.1897A>G	NP_000304.2:p.Asn633Asp
NM_001314077.1:c.1993A>G , LRG_572t2:c.1993A>G	NP_001301006.1:p.Asn665Asp
NM_000313.4:c.1897A>G MANE Select	NP_000304.2:p.Asn633Asp
NM_001314077.2:c.1993A>G	NP_001301006.1:p.Asn665Asp