Canonical Allele Identifier: CA1385042407
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs1708658201

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93905460_93905462del , CM000665.2:g.93905460_93905462del GRCh38
NC_000003.11:g.93624304_93624306del , CM000665.1:g.93624304_93624306del GRCh37
NC_000003.10:g.95106994_95106996del NCBI36
NG_009813.1:g.73630_73632del , LRG_572:g.73630_73632del

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.601+323_601+325del ENSP00000330021.7:n.601+323_601+325del
ENST00000394236.9:c.601+323_601+325del MANE Select ENSP00000377783.3:n.601+323_601+325del
ENST00000407433.6:c.556+368_556+370del ENSP00000385794.2:n.556+368_556+370del
ENST00000647936.1:c.601+323_601+325del ENSP00000496822.1:n.601+323_601+325del
ENST00000648381.1:n.769+323_769+325del
ENST00000648853.1:c.559+323_559+325del ENSP00000497262.1:n.559+323_559+325del
ENST00000649103.1:c.700+323_700+325del ENSP00000497962.1:n.700+323_700+325del
ENST00000650591.1:c.697+323_697+325del ENSP00000497376.1:n.697+323_697+325del
ENST00000394236.7:c.601+323_601+325del ENSP00000377783.3:n.601+323_601+325del
ENST00000407433.5:c.208+323_208+325del ENSP00000385794.1:n.208+323_208+325del
NM_000313.3:c.601+323_601+325del , LRG_572t1:c.601+323_601+325del NP_000304.2:n.601+323_601+325del
NM_001314077.1:c.697+323_697+325del , LRG_572t2:c.697+323_697+325del NP_001301006.1:n.697+323_697+325del
NM_000313.4:c.601+323_601+325del MANE Select NP_000304.2:n.601+323_601+325del
NM_001314077.2:c.697+323_697+325del NP_001301006.1:n.697+323_697+325del