Canonical Allele Identifier: CA353669355

Gene: PROS1

Linked Data

• gnomAD v4: 3-93874258-G-A
• MyVariant Identifiers: chr3:g.93593102G>A (hg19) ; chr3:g.93874258G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874258G>A , CM000665.2:g.93874258G>A	GRCh38
NC_000003.11:g.93593102G>A , CM000665.1:g.93593102G>A	GRCh37
NC_000003.10:g.95075792G>A	NCBI36
NG_009813.1:g.104833C>T , LRG_572:g.104833C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.2018C>T	ENSP00000330021.7:p.Thr673Ile
ENST00000394236.9:c.2018C>T MANE Select	ENSP00000377783.3:p.Thr673Ile
ENST00000407433.6:c.1973C>T	ENSP00000385794.2:p.Thr658Ile
ENST00000647936.1:c.*121C>T	ENSP00000496822.1:n.*121C>T
ENST00000648381.1:n.2186C>T
ENST00000648853.1:c.1976C>T	ENSP00000497262.1:p.Thr659Ile
ENST00000650591.1:c.2114C>T	ENSP00000497376.1:p.Thr705Ile
ENST00000394236.7:c.2018C>T	ENSP00000377783.3:p.Thr673Ile
ENST00000407433.5:c.1625C>T	ENSP00000385794.1:p.Thr542Ile
NM_000313.3:c.2018C>T , LRG_572t1:c.2018C>T	NP_000304.2:p.Thr673Ile
NM_001314077.1:c.2114C>T , LRG_572t2:c.2114C>T	NP_001301006.1:p.Thr705Ile
NM_000313.4:c.2018C>T MANE Select	NP_000304.2:p.Thr673Ile
NM_001314077.2:c.2114C>T	NP_001301006.1:p.Thr705Ile