Canonical Allele Identifier: CA2577828307

Gene: PROS1

Linked Data

• gnomAD v4: 3-93896517-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896517T>C , CM000665.2:g.93896517T>C	GRCh38
NC_000003.11:g.93615361T>C , CM000665.1:g.93615361T>C	GRCh37
NC_000003.10:g.95098051T>C	NCBI36
NG_009813.1:g.82574A>G , LRG_572:g.82574A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.965+59A>G	ENSP00000330021.7:n.965+59A>G
ENST00000394236.9:c.965+59A>G MANE Select	ENSP00000377783.3:n.965+59A>G
ENST00000407433.6:c.920+59A>G	ENSP00000385794.2:n.920+59A>G
ENST00000647936.1:c.965+59A>G	ENSP00000496822.1:n.965+59A>G
ENST00000648381.1:n.1133+59A>G
ENST00000648853.1:c.923+59A>G	ENSP00000497262.1:n.923+59A>G
ENST00000649103.1:c.1064+59A>G	ENSP00000497962.1:n.1064+59A>G
ENST00000650591.1:c.1061+59A>G	ENSP00000497376.1:n.1061+59A>G
ENST00000394236.7:c.965+59A>G	ENSP00000377783.3:n.965+59A>G
ENST00000407433.5:c.572+59A>G	ENSP00000385794.1:n.572+59A>G
NM_000313.3:c.965+59A>G , LRG_572t1:c.965+59A>G	NP_000304.2:n.965+59A>G
NM_001314077.1:c.1061+59A>G , LRG_572t2:c.1061+59A>G	NP_001301006.1:n.1061+59A>G
NM_000313.4:c.965+59A>G MANE Select	NP_000304.2:n.965+59A>G
NM_001314077.2:c.1061+59A>G	NP_001301006.1:n.1061+59A>G