Canonical Allele Identifier: CA434462860

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646181G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927337G>C , CM000665.2:g.93927337G>C	GRCh38
NC_000003.11:g.93646181G>C , CM000665.1:g.93646181G>C	GRCh37
NC_000003.10:g.95128871G>C	NCBI36
NG_009813.1:g.51754C>G , LRG_572:g.51754C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.147C>G	ENSP00000330021.7:p.Thr49=
ENST00000394236.9:c.147C>G MANE Select	ENSP00000377783.3:p.Thr49=
ENST00000407433.6:c.147C>G	ENSP00000385794.2:p.Thr49=
ENST00000472684.2:c.-247C>G	ENSP00000419616.2:n.-247C>G
ENST00000647936.1:c.147C>G	ENSP00000496822.1:p.Thr49=
ENST00000648381.1:n.315C>G
ENST00000648853.1:c.105C>G	ENSP00000497262.1:p.Thr35=
ENST00000649103.1:c.126C>G	ENSP00000497962.1:p.Thr42=
ENST00000650591.1:c.243C>G	ENSP00000497376.1:p.Thr81=
ENST00000348974.4:c.243C>G	ENSP00000330021.6:p.Thr81=
ENST00000394236.7:c.147C>G	ENSP00000377783.3:p.Thr49=
ENST00000407433.5:c.-247C>G	ENSP00000385794.1:n.-247C>G
ENST00000472684.1:c.-247C>G	ENSP00000419616.1:n.-247C>G
NM_000313.3:c.147C>G , LRG_572t1:c.147C>G	NP_000304.2:p.Thr49=
NM_001314077.1:c.243C>G , LRG_572t2:c.243C>G	NP_001301006.1:p.Thr81=
NM_000313.4:c.147C>G MANE Select	NP_000304.2:p.Thr49=
NM_001314077.2:c.243C>G	NP_001301006.1:p.Thr81=