Canonical Allele Identifier: CA2666653129

Gene: PROS1

Linked Data

• gnomAD v4: 3-93874184-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874184_93874185insC , CM000665.2:g.93874184_93874185insC	GRCh38
NC_000003.11:g.93593028_93593029insC , CM000665.1:g.93593028_93593029insC	GRCh37
NC_000003.10:g.95075718_95075719insC	NCBI36
NG_009813.1:g.104906_104907insG , LRG_572:g.104906_104907insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+59_*1+60insG	ENSP00000330021.7:n.*1+59_*1+60insG
ENST00000394236.9:c.*60_*61insG MANE Select	ENSP00000377783.3:n.*60_*61insG
ENST00000407433.6:c.*60_*61insG	ENSP00000385794.2:n.*60_*61insG
ENST00000647936.1:c.*194_*195insG	ENSP00000496822.1:n.*194_*195insG
ENST00000648381.1:n.2259_2260insG
ENST00000648853.1:c.*60_*61insG	ENSP00000497262.1:n.*60_*61insG
ENST00000650591.1:c.*60_*61insG	ENSP00000497376.1:n.*60_*61insG
ENST00000394236.7:c.*60_*61insG	ENSP00000377783.3:n.*60_*61insG
ENST00000407433.5:c.*60_*61insG	ENSP00000385794.1:n.*60_*61insG
NM_000313.3:c.*60_*61insG , LRG_572t1:c.*60_*61insG	NP_000304.2:n.*60_*61insG
NM_001314077.1:c.*60_*61insG , LRG_572t2:c.*60_*61insG	NP_001301006.1:n.*60_*61insG
NM_000313.4:c.*60_*61insG MANE Select	NP_000304.2:n.*60_*61insG
NM_001314077.2:c.*60_*61insG	NP_001301006.1:n.*60_*61insG