Canonical Allele Identifier: CA648275782

Gene: PROS1

Linked Data

• COSMIC: COSN19556853

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873821_93873822insC , CM000665.2:g.93873821_93873822insC	GRCh38
NC_000003.11:g.93592665_93592666insC , CM000665.1:g.93592665_93592666insC	GRCh37
NC_000003.10:g.95075355_95075356insC	NCBI36
NG_009813.1:g.105269_105270insG , LRG_572:g.105269_105270insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*2-409_*2-408insG	ENSP00000330021.7:n.*2-409_*2-408insG
ENST00000394236.9:c.*423_*424insG MANE Select	ENSP00000377783.3:n.*423_*424insG
ENST00000407433.6:c.*423_*424insG	ENSP00000385794.2:n.*423_*424insG
ENST00000647936.1:c.*557_*558insG	ENSP00000496822.1:n.*557_*558insG
ENST00000648381.1:n.2622_2623insG
ENST00000648853.1:c.*423_*424insG	ENSP00000497262.1:n.*423_*424insG
ENST00000650591.1:c.*423_*424insG	ENSP00000497376.1:n.*423_*424insG
ENST00000394236.7:c.*423_*424insG	ENSP00000377783.3:n.*423_*424insG
ENST00000407433.5:c.*423_*424insG	ENSP00000385794.1:n.*423_*424insG
NM_000313.3:c.*423_*424insG , LRG_572t1:c.*423_*424insG	NP_000304.2:n.*423_*424insG
NM_001314077.1:c.*423_*424insG , LRG_572t2:c.*423_*424insG	NP_001301006.1:n.*423_*424insG
NM_000313.4:c.*423_*424insG MANE Select	NP_000304.2:n.*423_*424insG
NM_001314077.2:c.*423_*424insG	NP_001301006.1:n.*423_*424insG