Canonical Allele Identifier: CA2757500461
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874447G>A , CM000665.2:g.93874447G>A GRCh38
NC_000003.11:g.93593291G>A , CM000665.1:g.93593291G>A GRCh37
NC_000003.10:g.95075981G>A NCBI36
NG_009813.1:g.104644C>T , LRG_572:g.104644C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1871-42C>T ENSP00000330021.7:n.1871-42C>T
ENST00000394236.9:c.1871-42C>T MANE Select ENSP00000377783.3:n.1871-42C>T
ENST00000407433.6:c.1826-42C>T ENSP00000385794.2:n.1826-42C>T
ENST00000647936.1:c.1645-42C>T ENSP00000496822.1:n.1645-42C>T
ENST00000648381.1:n.2039-42C>T
ENST00000648853.1:c.1829-42C>T ENSP00000497262.1:n.1829-42C>T
ENST00000650591.1:c.1967-42C>T ENSP00000497376.1:n.1967-42C>T
ENST00000394236.7:c.1871-42C>T ENSP00000377783.3:n.1871-42C>T
ENST00000407433.5:c.1478-42C>T ENSP00000385794.1:n.1478-42C>T
NM_000313.3:c.1871-42C>T , LRG_572t1:c.1871-42C>T NP_000304.2:n.1871-42C>T
NM_001314077.1:c.1967-42C>T , LRG_572t2:c.1967-42C>T NP_001301006.1:n.1967-42C>T
NM_000313.4:c.1871-42C>T MANE Select NP_000304.2:n.1871-42C>T
NM_001314077.2:c.1967-42C>T NP_001301006.1:n.1967-42C>T