Canonical Allele Identifier: CA353670901
Gene: PROS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93877009T>A , CM000665.2:g.93877009T>A GRCh38
NC_000003.11:g.93595853T>A , CM000665.1:g.93595853T>A GRCh37
NC_000003.10:g.95078543T>A NCBI36
NG_009813.1:g.102082A>T , LRG_572:g.102082A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1827A>T ENSP00000330021.7:p.Lys609Asn
ENST00000394236.9:c.1827A>T MANE Select ENSP00000377783.3:p.Lys609Asn
ENST00000407433.6:c.1782A>T ENSP00000385794.2:p.Lys594Asn
ENST00000647936.1:c.1644+2154A>T ENSP00000496822.1:n.1644+2154A>T
ENST00000648381.1:n.1995A>T
ENST00000648853.1:c.1785A>T ENSP00000497262.1:p.Lys595Asn
ENST00000649585.1:c.770A>T ENSP00000498163.1:n.770A>T
ENST00000650591.1:c.1923A>T ENSP00000497376.1:p.Lys641Asn
ENST00000394236.7:c.1827A>T ENSP00000377783.3:p.Lys609Asn
ENST00000407433.5:c.1434A>T ENSP00000385794.1:p.Lys478Asn
NM_000313.3:c.1827A>T , LRG_572t1:c.1827A>T NP_000304.2:p.Lys609Asn
NM_001314077.1:c.1923A>T , LRG_572t2:c.1923A>T NP_001301006.1:p.Lys641Asn
NM_000313.4:c.1827A>T MANE Select NP_000304.2:p.Lys609Asn
NM_001314077.2:c.1923A>T NP_001301006.1:p.Lys641Asn