Canonical Allele Identifier: CA1385042408
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93905459_93905460delinsGC , CM000665.2:g.93905459_93905460delinsGC GRCh38
NC_000003.11:g.93624303_93624304delinsGC , CM000665.1:g.93624303_93624304delinsGC GRCh37
NC_000003.10:g.95106993_95106994delinsGC NCBI36
NG_009813.1:g.73631_73632delinsGC , LRG_572:g.73631_73632delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.601+324_601+325delinsGC ENSP00000330021.7:n.601+324_601+325delinsGC
ENST00000394236.9:c.601+324_601+325delinsGC MANE Select ENSP00000377783.3:n.601+324_601+325delinsGC
ENST00000407433.6:c.556+369_556+370delinsGC ENSP00000385794.2:n.556+369_556+370delinsGC
ENST00000647936.1:c.601+324_601+325delinsGC ENSP00000496822.1:n.601+324_601+325delinsGC
ENST00000648381.1:n.769+324_769+325delinsGC
ENST00000648853.1:c.559+324_559+325delinsGC ENSP00000497262.1:n.559+324_559+325delinsGC
ENST00000649103.1:c.700+324_700+325delinsGC ENSP00000497962.1:n.700+324_700+325delinsGC
ENST00000650591.1:c.697+324_697+325delinsGC ENSP00000497376.1:n.697+324_697+325delinsGC
ENST00000394236.7:c.601+324_601+325delinsGC ENSP00000377783.3:n.601+324_601+325delinsGC
ENST00000407433.5:c.208+324_208+325delinsGC ENSP00000385794.1:n.208+324_208+325delinsGC
NM_000313.3:c.601+324_601+325delinsGC , LRG_572t1:c.601+324_601+325delinsGC NP_000304.2:n.601+324_601+325delinsGC
NM_001314077.1:c.697+324_697+325delinsGC , LRG_572t2:c.697+324_697+325delinsGC NP_001301006.1:n.697+324_697+325delinsGC
NM_000313.4:c.601+324_601+325delinsGC MANE Select NP_000304.2:n.601+324_601+325delinsGC
NM_001314077.2:c.697+324_697+325delinsGC NP_001301006.1:n.697+324_697+325delinsGC