Canonical Allele Identifier: CA1385038338

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896685_93896688delinsAAAC , CM000665.2:g.93896685_93896688delinsAAAC	GRCh38
NC_000003.11:g.93615529_93615532delinsAAAC , CM000665.1:g.93615529_93615532delinsAAAC	GRCh37
NC_000003.10:g.95098219_95098222delinsAAAC	NCBI36
NG_009813.1:g.82403_82406delinsGTTT , LRG_572:g.82403_82406delinsGTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.853_856delinsGTTT	ENSP00000330021.7:p.Val285=
ENST00000394236.9:c.853_856delinsGTTT MANE Select	ENSP00000377783.3:p.Val285=
ENST00000407433.6:c.808_811delinsGTTT	ENSP00000385794.2:p.Val270=
ENST00000647936.1:c.853_856delinsGTTT	ENSP00000496822.1:p.Val285=
ENST00000648381.1:n.1021_1024delinsGTTT
ENST00000648853.1:c.811_814delinsGTTT	ENSP00000497262.1:p.Val271=
ENST00000649103.1:c.952_955delinsGTTT	ENSP00000497962.1:n.952_955delinsGTTT
ENST00000650591.1:c.949_952delinsGTTT	ENSP00000497376.1:p.Val317=
ENST00000394236.7:c.853_856delinsGTTT	ENSP00000377783.3:p.Val285=
ENST00000407433.5:c.460_463delinsGTTT	ENSP00000385794.1:p.Val154=
NM_000313.3:c.853_856delinsGTTT , LRG_572t1:c.853_856delinsGTTT	NP_000304.2:p.Val285=
NM_001314077.1:c.949_952delinsGTTT , LRG_572t2:c.949_952delinsGTTT	NP_001301006.1:p.Val317=
NM_000313.4:c.853_856delinsGTTT MANE Select	NP_000304.2:p.Val285=
NM_001314077.2:c.949_952delinsGTTT	NP_001301006.1:p.Val317=