Canonical Allele Identifier: CA353674662

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646211C>G (hg19) ; chr3:g.93927367C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927367C>G , CM000665.2:g.93927367C>G	GRCh38
NC_000003.11:g.93646211C>G , CM000665.1:g.93646211C>G	GRCh37
NC_000003.10:g.95128901C>G	NCBI36
NG_009813.1:g.51724G>C , LRG_572:g.51724G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.117G>C	ENSP00000330021.7:p.Lys39Asn
ENST00000394236.9:c.117G>C MANE Select	ENSP00000377783.3:p.Lys39Asn
ENST00000407433.6:c.117G>C	ENSP00000385794.2:p.Lys39Asn
ENST00000472684.2:c.-277G>C	ENSP00000419616.2:n.-277G>C
ENST00000647936.1:c.117G>C	ENSP00000496822.1:p.Lys39Asn
ENST00000648381.1:n.285G>C
ENST00000648853.1:c.75G>C	ENSP00000497262.1:p.Lys25Asn
ENST00000649103.1:c.96G>C	ENSP00000497962.1:p.Lys32Asn
ENST00000650591.1:c.213G>C	ENSP00000497376.1:p.Lys71Asn
ENST00000348974.4:c.213G>C	ENSP00000330021.6:p.Lys71Asn
ENST00000394236.7:c.117G>C	ENSP00000377783.3:p.Lys39Asn
ENST00000407433.5:c.-277G>C	ENSP00000385794.1:n.-277G>C
ENST00000472684.1:c.-277G>C	ENSP00000419616.1:n.-277G>C
NM_000313.3:c.117G>C , LRG_572t1:c.117G>C	NP_000304.2:p.Lys39Asn
NM_001314077.1:c.213G>C , LRG_572t2:c.213G>C	NP_001301006.1:p.Lys71Asn
NM_000313.4:c.117G>C MANE Select	NP_000304.2:p.Lys39Asn
NM_001314077.2:c.213G>C	NP_001301006.1:p.Lys71Asn