Canonical Allele Identifier: CA1385042527
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93905701C= , CM000665.2:g.93905701C= GRCh38
NC_000003.11:g.93624545C= , CM000665.1:g.93624545C= GRCh37
NC_000003.10:g.95107235C= NCBI36
NG_009813.1:g.73390G= , LRG_572:g.73390G=

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.601+83G= ENSP00000330021.7:n.601+83G=
ENST00000394236.9:c.601+83G= MANE Select ENSP00000377783.3:n.601+83G=
ENST00000407433.6:c.556+128G= ENSP00000385794.2:n.556+128G=
ENST00000647936.1:c.601+83G= ENSP00000496822.1:n.601+83G=
ENST00000648381.1:n.769+83G=
ENST00000648853.1:c.559+83G= ENSP00000497262.1:n.559+83G=
ENST00000649103.1:c.700+83G= ENSP00000497962.1:n.700+83G=
ENST00000650591.1:c.697+83G= ENSP00000497376.1:n.697+83G=
ENST00000394236.7:c.601+83G= ENSP00000377783.3:n.601+83G=
ENST00000407433.5:c.208+83G= ENSP00000385794.1:n.208+83G=
NM_000313.3:c.601+83G= , LRG_572t1:c.601+83G= NP_000304.2:n.601+83G=
NM_001314077.1:c.697+83G= , LRG_572t2:c.697+83G= NP_001301006.1:n.697+83G=
NM_000313.4:c.601+83G= MANE Select NP_000304.2:n.601+83G=
NM_001314077.2:c.697+83G= NP_001301006.1:n.697+83G=