Canonical Allele Identifier: CA1385028964
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs1708200583

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93877054_93877055insAA , CM000665.2:g.93877054_93877055insAA GRCh38
NC_000003.11:g.93595898_93595899insAA , CM000665.1:g.93595898_93595899insAA GRCh37
NC_000003.10:g.95078588_95078589insAA NCBI36
NG_009813.1:g.102036_102037insTT , LRG_572:g.102036_102037insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1781_1782insTT ENSP00000330021.7:p.Ile595SerfsTer18
ENST00000394236.9:c.1781_1782insTT MANE Select ENSP00000377783.3:p.Ile595SerfsTer18
ENST00000407433.6:c.1736_1737insTT ENSP00000385794.2:p.Ile580SerfsTer18
ENST00000647936.1:c.1644+2108_1644+2109insTT ENSP00000496822.1:n.1644+2108_1644+2109insTT
ENST00000648381.1:n.1949_1950insTT
ENST00000648853.1:c.1739_1740insTT ENSP00000497262.1:p.Ile581SerfsTer18
ENST00000649103.1:c.1880_1881insTT ENSP00000497962.1:n.1880_1881insTT
ENST00000649585.1:c.724_725insTT ENSP00000498163.1:n.724_725insTT
ENST00000650591.1:c.1877_1878insTT ENSP00000497376.1:p.Ile627SerfsTer18
ENST00000394236.7:c.1781_1782insTT ENSP00000377783.3:p.Ile595SerfsTer18
ENST00000407433.5:c.1388_1389insTT ENSP00000385794.1:p.Ile464SerfsTer18
NM_000313.3:c.1781_1782insTT , LRG_572t1:c.1781_1782insTT NP_000304.2:p.Ile595SerfsTer18
NM_001314077.1:c.1877_1878insTT , LRG_572t2:c.1877_1878insTT NP_001301006.1:p.Ile627SerfsTer18
NM_000313.4:c.1781_1782insTT MANE Select NP_000304.2:p.Ile595SerfsTer18
NM_001314077.2:c.1877_1878insTT NP_001301006.1:p.Ile627SerfsTer18