Canonical Allele Identifier: CA1385030479
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs1708230624

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93878892_93878893del , CM000665.2:g.93878892_93878893del GRCh38
NC_000003.11:g.93597736_93597737del , CM000665.1:g.93597736_93597737del GRCh37
NC_000003.10:g.95080426_95080427del NCBI36
NG_009813.1:g.100201_100202del , LRG_572:g.100201_100202del

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1644+273_1644+274del ENSP00000330021.7:n.1644+273_1644+274del
ENST00000394236.9:c.1644+273_1644+274del MANE Select ENSP00000377783.3:n.1644+273_1644+274del
ENST00000407433.6:c.1599+273_1599+274del ENSP00000385794.2:n.1599+273_1599+274del
ENST00000647936.1:c.1644+273_1644+274del ENSP00000496822.1:n.1644+273_1644+274del
ENST00000648381.1:n.1812+273_1812+274del
ENST00000648853.1:c.1602+273_1602+274del ENSP00000497262.1:n.1602+273_1602+274del
ENST00000649103.1:c.1743+273_1743+274del ENSP00000497962.1:n.1743+273_1743+274del
ENST00000649585.1:c.587+273_587+274del ENSP00000498163.1:n.587+273_587+274del
ENST00000650591.1:c.1740+273_1740+274del ENSP00000497376.1:n.1740+273_1740+274del
ENST00000394236.7:c.1644+273_1644+274del ENSP00000377783.3:n.1644+273_1644+274del
ENST00000407433.5:c.1251+273_1251+274del ENSP00000385794.1:n.1251+273_1251+274del
NM_000313.3:c.1644+273_1644+274del , LRG_572t1:c.1644+273_1644+274del NP_000304.2:n.1644+273_1644+274del
NM_001314077.1:c.1740+273_1740+274del , LRG_572t2:c.1740+273_1740+274del NP_001301006.1:n.1740+273_1740+274del
NM_000313.4:c.1644+273_1644+274del MANE Select NP_000304.2:n.1644+273_1644+274del
NM_001314077.2:c.1740+273_1740+274del NP_001301006.1:n.1740+273_1740+274del