Canonical Allele Identifier: CA2577828456

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905748_93905749del , CM000665.2:g.93905748_93905749del	GRCh38
NC_000003.11:g.93624592_93624593del , CM000665.1:g.93624592_93624593del	GRCh37
NC_000003.10:g.95107282_95107283del	NCBI36
NG_009813.1:g.73342_73343del , LRG_572:g.73342_73343del

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.601+35_601+36del	ENSP00000330021.7:n.601+35_601+36del
ENST00000394236.9:c.601+35_601+36del MANE Select	ENSP00000377783.3:n.601+35_601+36del
ENST00000407433.6:c.556+80_556+81del	ENSP00000385794.2:n.556+80_556+81del
ENST00000647936.1:c.601+35_601+36del	ENSP00000496822.1:n.601+35_601+36del
ENST00000648381.1:n.769+35_769+36del
ENST00000648853.1:c.559+35_559+36del	ENSP00000497262.1:n.559+35_559+36del
ENST00000649103.1:c.700+35_700+36del	ENSP00000497962.1:n.700+35_700+36del
ENST00000650591.1:c.697+35_697+36del	ENSP00000497376.1:n.697+35_697+36del
ENST00000394236.7:c.601+35_601+36del	ENSP00000377783.3:n.601+35_601+36del
ENST00000407433.5:c.208+35_208+36del	ENSP00000385794.1:n.208+35_208+36del
NM_000313.3:c.601+35_601+36del , LRG_572t1:c.601+35_601+36del	NP_000304.2:n.601+35_601+36del
NM_001314077.1:c.697+35_697+36del , LRG_572t2:c.697+35_697+36del	NP_001301006.1:n.697+35_697+36del
NM_000313.4:c.601+35_601+36del MANE Select	NP_000304.2:n.601+35_601+36del
NM_001314077.2:c.697+35_697+36del	NP_001301006.1:n.697+35_697+36del