Canonical Allele Identifier: CA1385042519

Gene: PROS1

Linked Data

• dbSNP Id: rs1708663785

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905694_93905696del , CM000665.2:g.93905694_93905696del	GRCh38
NC_000003.11:g.93624538_93624540del , CM000665.1:g.93624538_93624540del	GRCh37
NC_000003.10:g.95107228_95107230del	NCBI36
NG_009813.1:g.73397_73399del , LRG_572:g.73397_73399del

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.601+90_601+92del	ENSP00000330021.7:n.601+90_601+92del
ENST00000394236.9:c.601+90_601+92del MANE Select	ENSP00000377783.3:n.601+90_601+92del
ENST00000407433.6:c.556+135_556+137del	ENSP00000385794.2:n.556+135_556+137del
ENST00000647936.1:c.601+90_601+92del	ENSP00000496822.1:n.601+90_601+92del
ENST00000648381.1:n.769+90_769+92del
ENST00000648853.1:c.559+90_559+92del	ENSP00000497262.1:n.559+90_559+92del
ENST00000649103.1:c.700+90_700+92del	ENSP00000497962.1:n.700+90_700+92del
ENST00000650591.1:c.697+90_697+92del	ENSP00000497376.1:n.697+90_697+92del
ENST00000394236.7:c.601+90_601+92del	ENSP00000377783.3:n.601+90_601+92del
ENST00000407433.5:c.208+90_208+92del	ENSP00000385794.1:n.208+90_208+92del
NM_000313.3:c.601+90_601+92del , LRG_572t1:c.601+90_601+92del	NP_000304.2:n.601+90_601+92del
NM_001314077.1:c.697+90_697+92del , LRG_572t2:c.697+90_697+92del	NP_001301006.1:n.697+90_697+92del
NM_000313.4:c.601+90_601+92del MANE Select	NP_000304.2:n.601+90_601+92del
NM_001314077.2:c.697+90_697+92del	NP_001301006.1:n.697+90_697+92del