Canonical Allele Identifier: CA2666657325

Gene: PROS1

Linked Data

• gnomAD v4: 3-93900733-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900733G>A , CM000665.2:g.93900733G>A	GRCh38
NC_000003.11:g.93619577G>A , CM000665.1:g.93619577G>A	GRCh37
NC_000003.10:g.95102267G>A	NCBI36
NG_009813.1:g.78358C>T , LRG_572:g.78358C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.727+71C>T	ENSP00000330021.7:n.727+71C>T
ENST00000394236.9:c.727+71C>T MANE Select	ENSP00000377783.3:n.727+71C>T
ENST00000407433.6:c.682+71C>T	ENSP00000385794.2:n.682+71C>T
ENST00000647936.1:c.727+71C>T	ENSP00000496822.1:n.727+71C>T
ENST00000648381.1:n.895+71C>T
ENST00000648853.1:c.685+71C>T	ENSP00000497262.1:n.685+71C>T
ENST00000649103.1:c.826+71C>T	ENSP00000497962.1:n.826+71C>T
ENST00000650591.1:c.823+71C>T	ENSP00000497376.1:n.823+71C>T
ENST00000394236.7:c.727+71C>T	ENSP00000377783.3:n.727+71C>T
ENST00000407433.5:c.334+71C>T	ENSP00000385794.1:n.334+71C>T
NM_000313.3:c.727+71C>T , LRG_572t1:c.727+71C>T	NP_000304.2:n.727+71C>T
NM_001314077.1:c.823+71C>T , LRG_572t2:c.823+71C>T	NP_001301006.1:n.823+71C>T
NM_000313.4:c.727+71C>T MANE Select	NP_000304.2:n.727+71C>T
NM_001314077.2:c.823+71C>T	NP_001301006.1:n.823+71C>T