Canonical Allele Identifier: CA912655341

Gene: PROS1

Linked Data

• dbSNP Id: rs1343890680
• gnomAD v3: 3-93905426-C-A
• gnomAD v4: 3-93905426-C-A
• MyVariant Identifiers: chr3:g.93624270C>A (hg19) ; chr3:g.93905426C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905426C>A , CM000665.2:g.93905426C>A	GRCh38
NC_000003.11:g.93624270C>A , CM000665.1:g.93624270C>A	GRCh37
NC_000003.10:g.95106960C>A	NCBI36
NG_009813.1:g.73665G>T , LRG_572:g.73665G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.601+358G>T	ENSP00000330021.7:n.601+358G>T
ENST00000394236.9:c.601+358G>T MANE Select	ENSP00000377783.3:n.601+358G>T
ENST00000407433.6:c.556+403G>T	ENSP00000385794.2:n.556+403G>T
ENST00000647936.1:c.601+358G>T	ENSP00000496822.1:n.601+358G>T
ENST00000648381.1:n.769+358G>T
ENST00000648853.1:c.559+358G>T	ENSP00000497262.1:n.559+358G>T
ENST00000649103.1:c.700+358G>T	ENSP00000497962.1:n.700+358G>T
ENST00000650591.1:c.697+358G>T	ENSP00000497376.1:n.697+358G>T
ENST00000394236.7:c.601+358G>T	ENSP00000377783.3:n.601+358G>T
ENST00000407433.5:c.208+358G>T	ENSP00000385794.1:n.208+358G>T
NM_000313.3:c.601+358G>T , LRG_572t1:c.601+358G>T	NP_000304.2:n.601+358G>T
NM_001314077.1:c.697+358G>T , LRG_572t2:c.697+358G>T	NP_001301006.1:n.697+358G>T
NM_000313.4:c.601+358G>T MANE Select	NP_000304.2:n.601+358G>T
NM_001314077.2:c.697+358G>T	NP_001301006.1:n.697+358G>T