Canonical Allele Identifier: CA1385038348

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896706_93896707delinsAC , CM000665.2:g.93896706_93896707delinsAC	GRCh38
NC_000003.11:g.93615550_93615551delinsAC , CM000665.1:g.93615550_93615551delinsAC	GRCh37
NC_000003.10:g.95098240_95098241delinsAC	NCBI36
NG_009813.1:g.82384_82385delinsGT , LRG_572:g.82384_82385delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.850-16_850-15delinsGT	ENSP00000330021.7:n.850-16_850-15delinsGT
ENST00000394236.9:c.850-16_850-15delinsGT MANE Select	ENSP00000377783.3:n.850-16_850-15delinsGT
ENST00000407433.6:c.805-16_805-15delinsGT	ENSP00000385794.2:n.805-16_805-15delinsGT
ENST00000647936.1:c.850-16_850-15delinsGT	ENSP00000496822.1:n.850-16_850-15delinsGT
ENST00000648381.1:n.1018-16_1018-15delinsGT
ENST00000648853.1:c.808-16_808-15delinsGT	ENSP00000497262.1:n.808-16_808-15delinsGT
ENST00000649103.1:c.949-16_949-15delinsGT	ENSP00000497962.1:n.949-16_949-15delinsGT
ENST00000650591.1:c.946-16_946-15delinsGT	ENSP00000497376.1:n.946-16_946-15delinsGT
ENST00000394236.7:c.850-16_850-15delinsGT	ENSP00000377783.3:n.850-16_850-15delinsGT
ENST00000407433.5:c.457-16_457-15delinsGT	ENSP00000385794.1:n.457-16_457-15delinsGT
NM_000313.3:c.850-16_850-15delinsGT , LRG_572t1:c.850-16_850-15delinsGT	NP_000304.2:n.850-16_850-15delinsGT
NM_001314077.1:c.946-16_946-15delinsGT , LRG_572t2:c.946-16_946-15delinsGT	NP_001301006.1:n.946-16_946-15delinsGT
NM_000313.4:c.850-16_850-15delinsGT MANE Select	NP_000304.2:n.850-16_850-15delinsGT
NM_001314077.2:c.946-16_946-15delinsGT	NP_001301006.1:n.946-16_946-15delinsGT