Canonical Allele Identifier: CA2666653123

Gene: PROS1

Linked Data

• gnomAD v4: 3-93874171-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874171A>G , CM000665.2:g.93874171A>G	GRCh38
NC_000003.11:g.93593015A>G , CM000665.1:g.93593015A>G	GRCh37
NC_000003.10:g.95075705A>G	NCBI36
NG_009813.1:g.104920T>C , LRG_572:g.104920T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.*1+73T>C	ENSP00000330021.7:n.*1+73T>C
ENST00000394236.9:c.*74T>C MANE Select	ENSP00000377783.3:n.*74T>C
ENST00000407433.6:c.*74T>C	ENSP00000385794.2:n.*74T>C
ENST00000647936.1:c.*208T>C	ENSP00000496822.1:n.*208T>C
ENST00000648381.1:n.2273T>C
ENST00000648853.1:c.*74T>C	ENSP00000497262.1:n.*74T>C
ENST00000650591.1:c.*74T>C	ENSP00000497376.1:n.*74T>C
ENST00000394236.7:c.*74T>C	ENSP00000377783.3:n.*74T>C
ENST00000407433.5:c.*74T>C	ENSP00000385794.1:n.*74T>C
NM_000313.3:c.*74T>C , LRG_572t1:c.*74T>C	NP_000304.2:n.*74T>C
NM_001314077.1:c.*74T>C , LRG_572t2:c.*74T>C	NP_001301006.1:n.*74T>C
NM_000313.4:c.*74T>C MANE Select	NP_000304.2:n.*74T>C
NM_001314077.2:c.*74T>C	NP_001301006.1:n.*74T>C