Canonical Allele Identifier: CA353671085

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93595909T>G (hg19) ; chr3:g.93877065T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877065T>G , CM000665.2:g.93877065T>G	GRCh38
NC_000003.11:g.93595909T>G , CM000665.1:g.93595909T>G	GRCh37
NC_000003.10:g.95078599T>G	NCBI36
NG_009813.1:g.102026A>C , LRG_572:g.102026A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1771A>C	ENSP00000330021.7:p.Lys591Gln
ENST00000394236.9:c.1771A>C MANE Select	ENSP00000377783.3:p.Lys591Gln
ENST00000407433.6:c.1726A>C	ENSP00000385794.2:p.Lys576Gln
ENST00000647936.1:c.1644+2098A>C	ENSP00000496822.1:n.1644+2098A>C
ENST00000648381.1:n.1939A>C
ENST00000648853.1:c.1729A>C	ENSP00000497262.1:p.Lys577Gln
ENST00000649103.1:c.1870A>C	ENSP00000497962.1:n.1870A>C
ENST00000649585.1:c.714A>C	ENSP00000498163.1:n.714A>C
ENST00000650591.1:c.1867A>C	ENSP00000497376.1:p.Lys623Gln
ENST00000394236.7:c.1771A>C	ENSP00000377783.3:p.Lys591Gln
ENST00000407433.5:c.1378A>C	ENSP00000385794.1:p.Lys460Gln
NM_000313.3:c.1771A>C , LRG_572t1:c.1771A>C	NP_000304.2:p.Lys591Gln
NM_001314077.1:c.1867A>C , LRG_572t2:c.1867A>C	NP_001301006.1:p.Lys623Gln
NM_000313.4:c.1771A>C MANE Select	NP_000304.2:p.Lys591Gln
NM_001314077.2:c.1867A>C	NP_001301006.1:p.Lys623Gln