Canonical Allele Identifier: CA353670850
Gene: PROS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93876984A>T , CM000665.2:g.93876984A>T GRCh38
NC_000003.11:g.93595828A>T , CM000665.1:g.93595828A>T GRCh37
NC_000003.10:g.95078518A>T NCBI36
NG_009813.1:g.102107T>A , LRG_572:g.102107T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1852T>A ENSP00000330021.7:p.Tyr618Asn
ENST00000394236.9:c.1852T>A MANE Select ENSP00000377783.3:p.Tyr618Asn
ENST00000407433.6:c.1807T>A ENSP00000385794.2:p.Tyr603Asn
ENST00000647936.1:c.1644+2179T>A ENSP00000496822.1:n.1644+2179T>A
ENST00000648381.1:n.2020T>A
ENST00000648853.1:c.1810T>A ENSP00000497262.1:p.Tyr604Asn
ENST00000650591.1:c.1948T>A ENSP00000497376.1:p.Tyr650Asn
ENST00000394236.7:c.1852T>A ENSP00000377783.3:p.Tyr618Asn
ENST00000407433.5:c.1459T>A ENSP00000385794.1:p.Tyr487Asn
NM_000313.3:c.1852T>A , LRG_572t1:c.1852T>A NP_000304.2:p.Tyr618Asn
NM_001314077.1:c.1948T>A , LRG_572t2:c.1948T>A NP_001301006.1:p.Tyr650Asn
NM_000313.4:c.1852T>A MANE Select NP_000304.2:p.Tyr618Asn
NM_001314077.2:c.1948T>A NP_001301006.1:p.Tyr650Asn