Canonical Allele Identifier: CA353672701

Gene: PROS1

Linked Data

• gnomAD v4: 3-93896666-T-A
• MyVariant Identifiers: chr3:g.93615510T>A (hg19) ; chr3:g.93896666T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896666T>A , CM000665.2:g.93896666T>A	GRCh38
NC_000003.11:g.93615510T>A , CM000665.1:g.93615510T>A	GRCh37
NC_000003.10:g.95098200T>A	NCBI36
NG_009813.1:g.82425A>T , LRG_572:g.82425A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.875A>T	ENSP00000330021.7:p.Asn292Ile
ENST00000394236.9:c.875A>T MANE Select	ENSP00000377783.3:p.Asn292Ile
ENST00000407433.6:c.830A>T	ENSP00000385794.2:p.Asn277Ile
ENST00000647936.1:c.875A>T	ENSP00000496822.1:p.Asn292Ile
ENST00000648381.1:n.1043A>T
ENST00000648853.1:c.833A>T	ENSP00000497262.1:p.Asn278Ile
ENST00000649103.1:c.974A>T	ENSP00000497962.1:n.974A>T
ENST00000650591.1:c.971A>T	ENSP00000497376.1:p.Asn324Ile
ENST00000394236.7:c.875A>T	ENSP00000377783.3:p.Asn292Ile
ENST00000407433.5:c.482A>T	ENSP00000385794.1:p.Asn161Ile
NM_000313.3:c.875A>T , LRG_572t1:c.875A>T	NP_000304.2:p.Asn292Ile
NM_001314077.1:c.971A>T , LRG_572t2:c.971A>T	NP_001301006.1:p.Asn324Ile
NM_000313.4:c.875A>T MANE Select	NP_000304.2:p.Asn292Ile
NM_001314077.2:c.971A>T	NP_001301006.1:p.Asn324Ile