Canonical Allele Identifier: CA1385042533
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93905710T= , CM000665.2:g.93905710T= GRCh38
NC_000003.11:g.93624554T= , CM000665.1:g.93624554T= GRCh37
NC_000003.10:g.95107244T= NCBI36
NG_009813.1:g.73381A= , LRG_572:g.73381A=

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.601+74A= ENSP00000330021.7:n.601+74A=
ENST00000394236.9:c.601+74A= MANE Select ENSP00000377783.3:n.601+74A=
ENST00000407433.6:c.556+119A= ENSP00000385794.2:n.556+119A=
ENST00000647936.1:c.601+74A= ENSP00000496822.1:n.601+74A=
ENST00000648381.1:n.769+74A=
ENST00000648853.1:c.559+74A= ENSP00000497262.1:n.559+74A=
ENST00000649103.1:c.700+74A= ENSP00000497962.1:n.700+74A=
ENST00000650591.1:c.697+74A= ENSP00000497376.1:n.697+74A=
ENST00000394236.7:c.601+74A= ENSP00000377783.3:n.601+74A=
ENST00000407433.5:c.208+74A= ENSP00000385794.1:n.208+74A=
NM_000313.3:c.601+74A= , LRG_572t1:c.601+74A= NP_000304.2:n.601+74A=
NM_001314077.1:c.697+74A= , LRG_572t2:c.697+74A= NP_001301006.1:n.697+74A=
NM_000313.4:c.601+74A= MANE Select NP_000304.2:n.601+74A=
NM_001314077.2:c.697+74A= NP_001301006.1:n.697+74A=