Canonical Allele Identifier: CA2666653075

Gene: PROS1

Linked Data

• gnomAD v4: 3-93874076-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874076T>A , CM000665.2:g.93874076T>A	GRCh38
NC_000003.11:g.93592920T>A , CM000665.1:g.93592920T>A	GRCh37
NC_000003.10:g.95075610T>A	NCBI36
NG_009813.1:g.105015A>T , LRG_572:g.105015A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+168A>T	ENSP00000330021.7:n.*1+168A>T
ENST00000394236.9:c.*169A>T MANE Select	ENSP00000377783.3:n.*169A>T
ENST00000407433.6:c.*169A>T	ENSP00000385794.2:n.*169A>T
ENST00000647936.1:c.*303A>T	ENSP00000496822.1:n.*303A>T
ENST00000648381.1:n.2368A>T
ENST00000648853.1:c.*169A>T	ENSP00000497262.1:n.*169A>T
ENST00000650591.1:c.*169A>T	ENSP00000497376.1:n.*169A>T
ENST00000394236.7:c.*169A>T	ENSP00000377783.3:n.*169A>T
ENST00000407433.5:c.*169A>T	ENSP00000385794.1:n.*169A>T
NM_000313.3:c.*169A>T , LRG_572t1:c.*169A>T	NP_000304.2:n.*169A>T
NM_001314077.1:c.*169A>T , LRG_572t2:c.*169A>T	NP_001301006.1:n.*169A>T
NM_000313.4:c.*169A>T MANE Select	NP_000304.2:n.*169A>T
NM_001314077.2:c.*169A>T	NP_001301006.1:n.*169A>T