Canonical Allele Identifier: CA353672350

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93611904G>A (hg19) ; chr3:g.93893060G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893060G>A , CM000665.2:g.93893060G>A	GRCh38
NC_000003.11:g.93611904G>A , CM000665.1:g.93611904G>A	GRCh37
NC_000003.10:g.95094594G>A	NCBI36
NG_009813.1:g.86031C>T , LRG_572:g.86031C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1028C>T	ENSP00000330021.7:p.Ser343Phe
ENST00000394236.9:c.1028C>T MANE Select	ENSP00000377783.3:p.Ser343Phe
ENST00000407433.6:c.983C>T	ENSP00000385794.2:p.Ser328Phe
ENST00000647936.1:c.1028C>T	ENSP00000496822.1:p.Ser343Phe
ENST00000648381.1:n.1196C>T
ENST00000648853.1:c.986C>T	ENSP00000497262.1:p.Ser329Phe
ENST00000649103.1:c.1127C>T	ENSP00000497962.1:n.1127C>T
ENST00000650591.1:c.1124C>T	ENSP00000497376.1:p.Ser375Phe
ENST00000394236.7:c.1028C>T	ENSP00000377783.3:p.Ser343Phe
ENST00000407433.5:c.635C>T	ENSP00000385794.1:p.Ser212Phe
NM_000313.3:c.1028C>T , LRG_572t1:c.1028C>T	NP_000304.2:p.Ser343Phe
NM_001314077.1:c.1124C>T , LRG_572t2:c.1124C>T	NP_001301006.1:p.Ser375Phe
NM_000313.4:c.1028C>T MANE Select	NP_000304.2:p.Ser343Phe
NM_001314077.2:c.1124C>T	NP_001301006.1:p.Ser375Phe