Canonical Allele Identifier: CA1385029375
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93877157T= , CM000665.2:g.93877157T= GRCh38
NC_000003.11:g.93596001T= , CM000665.1:g.93596001T= GRCh37
NC_000003.10:g.95078691T= NCBI36
NG_009813.1:g.101934A= , LRG_572:g.101934A=

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.1679A= ENSP00000330021.7:p.Tyr560=
ENST00000394236.9:c.1679A= MANE Select ENSP00000377783.3:p.Tyr560=
ENST00000407433.6:c.1634A= ENSP00000385794.2:p.Tyr545=
ENST00000647936.1:c.1644+2006A= ENSP00000496822.1:n.1644+2006A=
ENST00000648381.1:n.1847A=
ENST00000648853.1:c.1637A= ENSP00000497262.1:p.Tyr546=
ENST00000649103.1:c.1778A= ENSP00000497962.1:n.1778A=
ENST00000649585.1:c.622A= ENSP00000498163.1:n.622A=
ENST00000650591.1:c.1775A= ENSP00000497376.1:p.Tyr592=
ENST00000394236.7:c.1679A= ENSP00000377783.3:p.Tyr560=
ENST00000407433.5:c.1286A= ENSP00000385794.1:p.Tyr429=
NM_000313.3:c.1679A= , LRG_572t1:c.1679A= NP_000304.2:p.Tyr560=
NM_001314077.1:c.1775A= , LRG_572t2:c.1775A= NP_001301006.1:p.Tyr592=
NM_000313.4:c.1679A= MANE Select NP_000304.2:p.Tyr560=
NM_001314077.2:c.1775A= NP_001301006.1:p.Tyr592=