Canonical Allele Identifier: CA353672681

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615501G>C (hg19) ; chr3:g.93896657G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896657G>C , CM000665.2:g.93896657G>C	GRCh38
NC_000003.11:g.93615501G>C , CM000665.1:g.93615501G>C	GRCh37
NC_000003.10:g.95098191G>C	NCBI36
NG_009813.1:g.82434C>G , LRG_572:g.82434C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.884C>G	ENSP00000330021.7:p.Thr295Arg
ENST00000394236.9:c.884C>G MANE Select	ENSP00000377783.3:p.Thr295Arg
ENST00000407433.6:c.839C>G	ENSP00000385794.2:p.Thr280Arg
ENST00000647936.1:c.884C>G	ENSP00000496822.1:p.Thr295Arg
ENST00000648381.1:n.1052C>G
ENST00000648853.1:c.842C>G	ENSP00000497262.1:p.Thr281Arg
ENST00000649103.1:c.983C>G	ENSP00000497962.1:n.983C>G
ENST00000650591.1:c.980C>G	ENSP00000497376.1:p.Thr327Arg
ENST00000394236.7:c.884C>G	ENSP00000377783.3:p.Thr295Arg
ENST00000407433.5:c.491C>G	ENSP00000385794.1:p.Thr164Arg
NM_000313.3:c.884C>G , LRG_572t1:c.884C>G	NP_000304.2:p.Thr295Arg
NM_001314077.1:c.980C>G , LRG_572t2:c.980C>G	NP_001301006.1:p.Thr327Arg
NM_000313.4:c.884C>G MANE Select	NP_000304.2:p.Thr295Arg
NM_001314077.2:c.980C>G	NP_001301006.1:p.Thr327Arg