Canonical Allele Identifier: CA1385042481
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93905600_93905602delinsATC , CM000665.2:g.93905600_93905602delinsATC GRCh38
NC_000003.11:g.93624444_93624446delinsATC , CM000665.1:g.93624444_93624446delinsATC GRCh37
NC_000003.10:g.95107134_95107136delinsATC NCBI36
NG_009813.1:g.73489_73491delinsGAT , LRG_572:g.73489_73491delinsGAT

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.601+182_601+184delinsGAT ENSP00000330021.7:n.601+182_601+184delinsGAT
ENST00000394236.9:c.601+182_601+184delinsGAT MANE Select ENSP00000377783.3:n.601+182_601+184delinsGAT
ENST00000407433.6:c.556+227_556+229delinsGAT ENSP00000385794.2:n.556+227_556+229delinsGAT
ENST00000647936.1:c.601+182_601+184delinsGAT ENSP00000496822.1:n.601+182_601+184delinsGAT
ENST00000648381.1:n.769+182_769+184delinsGAT
ENST00000648853.1:c.559+182_559+184delinsGAT ENSP00000497262.1:n.559+182_559+184delinsGAT
ENST00000649103.1:c.700+182_700+184delinsGAT ENSP00000497962.1:n.700+182_700+184delinsGAT
ENST00000650591.1:c.697+182_697+184delinsGAT ENSP00000497376.1:n.697+182_697+184delinsGAT
ENST00000394236.7:c.601+182_601+184delinsGAT ENSP00000377783.3:n.601+182_601+184delinsGAT
ENST00000407433.5:c.208+182_208+184delinsGAT ENSP00000385794.1:n.208+182_208+184delinsGAT
NM_000313.3:c.601+182_601+184delinsGAT , LRG_572t1:c.601+182_601+184delinsGAT NP_000304.2:n.601+182_601+184delinsGAT
NM_001314077.1:c.697+182_697+184delinsGAT , LRG_572t2:c.697+182_697+184delinsGAT NP_001301006.1:n.697+182_697+184delinsGAT
NM_000313.4:c.601+182_601+184delinsGAT MANE Select NP_000304.2:n.601+182_601+184delinsGAT
NM_001314077.2:c.697+182_697+184delinsGAT NP_001301006.1:n.697+182_697+184delinsGAT