Canonical Allele Identifier: CA1385059426

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927330_93927332delinsCCT , CM000665.2:g.93927330_93927332delinsCCT	GRCh38
NC_000003.11:g.93646174_93646176delinsCCT , CM000665.1:g.93646174_93646176delinsCCT	GRCh37
NC_000003.10:g.95128864_95128866delinsCCT	NCBI36
NG_009813.1:g.51759_51761delinsAGG , LRG_572:g.51759_51761delinsAGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.152_154delinsAGG	ENSP00000330021.7:p.Gln51=
ENST00000394236.9:c.152_154delinsAGG MANE Select	ENSP00000377783.3:p.Gln51=
ENST00000407433.6:c.152_154delinsAGG	ENSP00000385794.2:p.Gln51=
ENST00000472684.2:c.-242_-240delinsAGG	ENSP00000419616.2:n.-242_-240delinsAGG
ENST00000647936.1:c.152_154delinsAGG	ENSP00000496822.1:p.Gln51=
ENST00000648381.1:n.320_322delinsAGG
ENST00000648853.1:c.110_112delinsAGG	ENSP00000497262.1:p.Gln37=
ENST00000649103.1:c.131_133delinsAGG	ENSP00000497962.1:p.Gln44=
ENST00000650591.1:c.248_250delinsAGG	ENSP00000497376.1:p.Gln83=
ENST00000348974.4:c.248_250delinsAGG	ENSP00000330021.6:p.Gln83=
ENST00000394236.7:c.152_154delinsAGG	ENSP00000377783.3:p.Gln51=
ENST00000407433.5:c.-242_-240delinsAGG	ENSP00000385794.1:n.-242_-240delinsAGG
ENST00000472684.1:c.-242_-240delinsAGG	ENSP00000419616.1:n.-242_-240delinsAGG
NM_000313.3:c.152_154delinsAGG , LRG_572t1:c.152_154delinsAGG	NP_000304.2:p.Gln51=
NM_001314077.1:c.248_250delinsAGG , LRG_572t2:c.248_250delinsAGG	NP_001301006.1:p.Gln83=
NM_000313.4:c.152_154delinsAGG MANE Select	NP_000304.2:p.Gln51=
NM_001314077.2:c.248_250delinsAGG	NP_001301006.1:p.Gln83=