Canonical Allele Identifier: CA2666652942

Gene: PROS1

Linked Data

• gnomAD v4: 3-93873806-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873806C>T , CM000665.2:g.93873806C>T	GRCh38
NC_000003.11:g.93592650C>T , CM000665.1:g.93592650C>T	GRCh37
NC_000003.10:g.95075340C>T	NCBI36
NG_009813.1:g.105285G>A , LRG_572:g.105285G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*2-393G>A	ENSP00000330021.7:n.*2-393G>A
ENST00000394236.9:c.*439G>A MANE Select	ENSP00000377783.3:n.*439G>A
ENST00000407433.6:c.*439G>A	ENSP00000385794.2:n.*439G>A
ENST00000647936.1:c.*573G>A	ENSP00000496822.1:n.*573G>A
ENST00000648381.1:n.2638G>A
ENST00000648853.1:c.*439G>A	ENSP00000497262.1:n.*439G>A
ENST00000650591.1:c.*439G>A	ENSP00000497376.1:n.*439G>A
ENST00000394236.7:c.*439G>A	ENSP00000377783.3:n.*439G>A
ENST00000407433.5:c.*439G>A	ENSP00000385794.1:n.*439G>A
NM_000313.3:c.*439G>A , LRG_572t1:c.*439G>A	NP_000304.2:n.*439G>A
NM_001314077.1:c.*439G>A , LRG_572t2:c.*439G>A	NP_001301006.1:n.*439G>A
NM_000313.4:c.*439G>A MANE Select	NP_000304.2:n.*439G>A
NM_001314077.2:c.*439G>A	NP_001301006.1:n.*439G>A