Canonical Allele Identifier: CA353671844

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598057T>G (hg19) ; chr3:g.93879213T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879213T>G , CM000665.2:g.93879213T>G	GRCh38
NC_000003.11:g.93598057T>G , CM000665.1:g.93598057T>G	GRCh37
NC_000003.10:g.95080747T>G	NCBI36
NG_009813.1:g.99878A>C , LRG_572:g.99878A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1594A>C	ENSP00000330021.7:p.Thr532Pro
ENST00000394236.9:c.1594A>C MANE Select	ENSP00000377783.3:p.Thr532Pro
ENST00000407433.6:c.1549A>C	ENSP00000385794.2:p.Thr517Pro
ENST00000647936.1:c.1594A>C	ENSP00000496822.1:p.Thr532Pro
ENST00000648381.1:n.1762A>C
ENST00000648853.1:c.1552A>C	ENSP00000497262.1:p.Thr518Pro
ENST00000649103.1:c.1693A>C	ENSP00000497962.1:n.1693A>C
ENST00000649585.1:c.537A>C	ENSP00000498163.1:n.537A>C
ENST00000650591.1:c.1690A>C	ENSP00000497376.1:p.Thr564Pro
ENST00000394236.7:c.1594A>C	ENSP00000377783.3:p.Thr532Pro
ENST00000407433.5:c.1201A>C	ENSP00000385794.1:p.Thr401Pro
NM_000313.3:c.1594A>C , LRG_572t1:c.1594A>C	NP_000304.2:p.Thr532Pro
NM_001314077.1:c.1690A>C , LRG_572t2:c.1690A>C	NP_001301006.1:p.Thr564Pro
NM_000313.4:c.1594A>C MANE Select	NP_000304.2:p.Thr532Pro
NM_001314077.2:c.1690A>C	NP_001301006.1:p.Thr564Pro