Canonical Allele Identifier: CA353673089

Gene: PROS1

Linked Data

• COSMIC: COSM366436
• MyVariant Identifiers: chr3:g.93619658C>A (hg19) ; chr3:g.93900814C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900814C>A , CM000665.2:g.93900814C>A	GRCh38
NC_000003.11:g.93619658C>A , CM000665.1:g.93619658C>A	GRCh37
NC_000003.10:g.95102348C>A	NCBI36
NG_009813.1:g.78277G>T , LRG_572:g.78277G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.717G>T	ENSP00000330021.7:p.Lys239Asn
ENST00000394236.9:c.717G>T MANE Select	ENSP00000377783.3:p.Lys239Asn
ENST00000407433.6:c.672G>T	ENSP00000385794.2:p.Lys224Asn
ENST00000647936.1:c.717G>T	ENSP00000496822.1:p.Lys239Asn
ENST00000648381.1:n.885G>T
ENST00000648853.1:c.675G>T	ENSP00000497262.1:p.Lys225Asn
ENST00000649103.1:c.816G>T	ENSP00000497962.1:n.816G>T
ENST00000650591.1:c.813G>T	ENSP00000497376.1:p.Lys271Asn
ENST00000394236.7:c.717G>T	ENSP00000377783.3:p.Lys239Asn
ENST00000407433.5:c.324G>T	ENSP00000385794.1:p.Lys108Asn
NM_000313.3:c.717G>T , LRG_572t1:c.717G>T	NP_000304.2:p.Lys239Asn
NM_001314077.1:c.813G>T , LRG_572t2:c.813G>T	NP_001301006.1:p.Lys271Asn
NM_000313.4:c.717G>T MANE Select	NP_000304.2:p.Lys239Asn
NM_001314077.2:c.813G>T	NP_001301006.1:p.Lys271Asn