Canonical Allele Identifier: CA353672849

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93617328T>G (hg19) ; chr3:g.93898484T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898484T>G , CM000665.2:g.93898484T>G	GRCh38
NC_000003.11:g.93617328T>G , CM000665.1:g.93617328T>G	GRCh37
NC_000003.10:g.95100018T>G	NCBI36
NG_009813.1:g.80607A>C , LRG_572:g.80607A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.813A>C	ENSP00000330021.7:p.Lys271Asn
ENST00000394236.9:c.813A>C MANE Select	ENSP00000377783.3:p.Lys271Asn
ENST00000407433.6:c.768A>C	ENSP00000385794.2:p.Lys256Asn
ENST00000647936.1:c.813A>C	ENSP00000496822.1:p.Lys271Asn
ENST00000648381.1:n.981A>C
ENST00000648853.1:c.771A>C	ENSP00000497262.1:p.Lys257Asn
ENST00000649103.1:c.912A>C	ENSP00000497962.1:n.912A>C
ENST00000650591.1:c.909A>C	ENSP00000497376.1:p.Lys303Asn
ENST00000394236.7:c.813A>C	ENSP00000377783.3:p.Lys271Asn
ENST00000407433.5:c.420A>C	ENSP00000385794.1:p.Lys140Asn
NM_000313.3:c.813A>C , LRG_572t1:c.813A>C	NP_000304.2:p.Lys271Asn
NM_001314077.1:c.909A>C , LRG_572t2:c.909A>C	NP_001301006.1:p.Lys303Asn
NM_000313.4:c.813A>C MANE Select	NP_000304.2:p.Lys271Asn
NM_001314077.2:c.909A>C	NP_001301006.1:p.Lys303Asn