Canonical Allele Identifier: CA1385039049

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898314_93898315delinsCT , CM000665.2:g.93898314_93898315delinsCT	GRCh38
NC_000003.11:g.93617158_93617159delinsCT , CM000665.1:g.93617158_93617159delinsCT	GRCh37
NC_000003.10:g.95099848_95099849delinsCT	NCBI36
NG_009813.1:g.80776_80777delinsAG , LRG_572:g.80776_80777delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.849+133_849+134delinsAG	ENSP00000330021.7:n.849+133_849+134delinsAG
ENST00000394236.9:c.849+133_849+134delinsAG MANE Select	ENSP00000377783.3:n.849+133_849+134delinsAG
ENST00000407433.6:c.804+133_804+134delinsAG	ENSP00000385794.2:n.804+133_804+134delinsAG
ENST00000647936.1:c.849+133_849+134delinsAG	ENSP00000496822.1:n.849+133_849+134delinsAG
ENST00000648381.1:n.1017+133_1017+134delinsAG
ENST00000648853.1:c.807+133_807+134delinsAG	ENSP00000497262.1:n.807+133_807+134delinsAG
ENST00000649103.1:c.948+133_948+134delinsAG	ENSP00000497962.1:n.948+133_948+134delinsAG
ENST00000650591.1:c.945+133_945+134delinsAG	ENSP00000497376.1:n.945+133_945+134delinsAG
ENST00000394236.7:c.849+133_849+134delinsAG	ENSP00000377783.3:n.849+133_849+134delinsAG
ENST00000407433.5:c.456+133_456+134delinsAG	ENSP00000385794.1:n.456+133_456+134delinsAG
NM_000313.3:c.849+133_849+134delinsAG , LRG_572t1:c.849+133_849+134delinsAG	NP_000304.2:n.849+133_849+134delinsAG
NM_001314077.1:c.945+133_945+134delinsAG , LRG_572t2:c.945+133_945+134delinsAG	NP_001301006.1:n.945+133_945+134delinsAG
NM_000313.4:c.849+133_849+134delinsAG MANE Select	NP_000304.2:n.849+133_849+134delinsAG
NM_001314077.2:c.945+133_945+134delinsAG	NP_001301006.1:n.945+133_945+134delinsAG