Canonical Allele Identifier: CA2666657486

Gene: PROS1

Linked Data

• gnomAD v4: 3-93905734-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905734G>C , CM000665.2:g.93905734G>C	GRCh38
NC_000003.11:g.93624578G>C , CM000665.1:g.93624578G>C	GRCh37
NC_000003.10:g.95107268G>C	NCBI36
NG_009813.1:g.73357C>G , LRG_572:g.73357C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.601+50C>G	ENSP00000330021.7:n.601+50C>G
ENST00000394236.9:c.601+50C>G MANE Select	ENSP00000377783.3:n.601+50C>G
ENST00000407433.6:c.556+95C>G	ENSP00000385794.2:n.556+95C>G
ENST00000647936.1:c.601+50C>G	ENSP00000496822.1:n.601+50C>G
ENST00000648381.1:n.769+50C>G
ENST00000648853.1:c.559+50C>G	ENSP00000497262.1:n.559+50C>G
ENST00000649103.1:c.700+50C>G	ENSP00000497962.1:n.700+50C>G
ENST00000650591.1:c.697+50C>G	ENSP00000497376.1:n.697+50C>G
ENST00000394236.7:c.601+50C>G	ENSP00000377783.3:n.601+50C>G
ENST00000407433.5:c.208+50C>G	ENSP00000385794.1:n.208+50C>G
NM_000313.3:c.601+50C>G , LRG_572t1:c.601+50C>G	NP_000304.2:n.601+50C>G
NM_001314077.1:c.697+50C>G , LRG_572t2:c.697+50C>G	NP_001301006.1:n.697+50C>G
NM_000313.4:c.601+50C>G MANE Select	NP_000304.2:n.601+50C>G
NM_001314077.2:c.697+50C>G	NP_001301006.1:n.697+50C>G