Canonical Allele Identifier: CA1385039128

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898511_93898512delinsAC , CM000665.2:g.93898511_93898512delinsAC	GRCh38
NC_000003.11:g.93617355_93617356delinsAC , CM000665.1:g.93617355_93617356delinsAC	GRCh37
NC_000003.10:g.95100045_95100046delinsAC	NCBI36
NG_009813.1:g.80579_80580delinsGT , LRG_572:g.80579_80580delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.785_786delinsGT	ENSP00000330021.7:p.Gly262=
ENST00000394236.9:c.785_786delinsGT MANE Select	ENSP00000377783.3:p.Gly262=
ENST00000407433.6:c.740_741delinsGT	ENSP00000385794.2:p.Gly247=
ENST00000647936.1:c.785_786delinsGT	ENSP00000496822.1:p.Gly262=
ENST00000648381.1:n.953_954delinsGT
ENST00000648853.1:c.743_744delinsGT	ENSP00000497262.1:p.Gly248=
ENST00000649103.1:c.884_885delinsGT	ENSP00000497962.1:n.884_885delinsGT
ENST00000650591.1:c.881_882delinsGT	ENSP00000497376.1:p.Gly294=
ENST00000394236.7:c.785_786delinsGT	ENSP00000377783.3:p.Gly262=
ENST00000407433.5:c.392_393delinsGT	ENSP00000385794.1:p.Gly131=
NM_000313.3:c.785_786delinsGT , LRG_572t1:c.785_786delinsGT	NP_000304.2:p.Gly262=
NM_001314077.1:c.881_882delinsGT , LRG_572t2:c.881_882delinsGT	NP_001301006.1:p.Gly294=
NM_000313.4:c.785_786delinsGT MANE Select	NP_000304.2:p.Gly262=
NM_001314077.2:c.881_882delinsGT	NP_001301006.1:p.Gly294=