Canonical Allele Identifier: CA914796902

Gene: PROS1

Linked Data

• gnomAD v2: 3-93598273-C-A
• gnomAD v4: 3-93879429-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879429C>A , CM000665.2:g.93879429C>A	GRCh38
NC_000003.11:g.93598273C>A , CM000665.1:g.93598273C>A	GRCh37
NC_000003.10:g.95080963C>A	NCBI36
NG_009813.1:g.99662G>T , LRG_572:g.99662G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1493-115G>T	ENSP00000330021.7:n.1493-115G>T
ENST00000394236.9:c.1493-115G>T MANE Select	ENSP00000377783.3:n.1493-115G>T
ENST00000407433.6:c.1448-115G>T	ENSP00000385794.2:n.1448-115G>T
ENST00000647936.1:c.1493-115G>T	ENSP00000496822.1:n.1493-115G>T
ENST00000648381.1:n.1661-115G>T
ENST00000648853.1:c.1451-115G>T	ENSP00000497262.1:n.1451-115G>T
ENST00000649103.1:c.1592-115G>T	ENSP00000497962.1:n.1592-115G>T
ENST00000649585.1:c.436-115G>T	ENSP00000498163.1:n.436-115G>T
ENST00000650591.1:c.1589-115G>T	ENSP00000497376.1:n.1589-115G>T
ENST00000394236.7:c.1493-115G>T	ENSP00000377783.3:n.1493-115G>T
ENST00000407433.5:c.1100-115G>T	ENSP00000385794.1:n.1100-115G>T
NM_000313.3:c.1493-115G>T , LRG_572t1:c.1493-115G>T	NP_000304.2:n.1493-115G>T
NM_001314077.1:c.1589-115G>T , LRG_572t2:c.1589-115G>T	NP_001301006.1:n.1589-115G>T
NM_000313.4:c.1493-115G>T MANE Select	NP_000304.2:n.1493-115G>T
NM_001314077.2:c.1589-115G>T	NP_001301006.1:n.1589-115G>T