Canonical Allele Identifier: CA353674604

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646182G>T (hg19) ; chr3:g.93927338G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927338G>T , CM000665.2:g.93927338G>T	GRCh38
NC_000003.11:g.93646182G>T , CM000665.1:g.93646182G>T	GRCh37
NC_000003.10:g.95128872G>T	NCBI36
NG_009813.1:g.51753C>A , LRG_572:g.51753C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.146C>A	ENSP00000330021.7:p.Thr49Asn
ENST00000394236.9:c.146C>A MANE Select	ENSP00000377783.3:p.Thr49Asn
ENST00000407433.6:c.146C>A	ENSP00000385794.2:p.Thr49Asn
ENST00000472684.2:c.-248C>A	ENSP00000419616.2:n.-248C>A
ENST00000647936.1:c.146C>A	ENSP00000496822.1:p.Thr49Asn
ENST00000648381.1:n.314C>A
ENST00000648853.1:c.104C>A	ENSP00000497262.1:p.Thr35Asn
ENST00000649103.1:c.125C>A	ENSP00000497962.1:p.Thr42Asn
ENST00000650591.1:c.242C>A	ENSP00000497376.1:p.Thr81Asn
ENST00000348974.4:c.242C>A	ENSP00000330021.6:p.Thr81Asn
ENST00000394236.7:c.146C>A	ENSP00000377783.3:p.Thr49Asn
ENST00000407433.5:c.-248C>A	ENSP00000385794.1:n.-248C>A
ENST00000472684.1:c.-248C>A	ENSP00000419616.1:n.-248C>A
NM_000313.3:c.146C>A , LRG_572t1:c.146C>A	NP_000304.2:p.Thr49Asn
NM_001314077.1:c.242C>A , LRG_572t2:c.242C>A	NP_001301006.1:p.Thr81Asn
NM_000313.4:c.146C>A MANE Select	NP_000304.2:p.Thr49Asn
NM_001314077.2:c.242C>A	NP_001301006.1:p.Thr81Asn