Canonical Allele Identifier: CA353670982

Gene: PROS1

Linked Data

• gnomAD v4: 3-93877040-T-C
• MyVariant Identifiers: chr3:g.93595884T>C (hg19) ; chr3:g.93877040T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877040T>C , CM000665.2:g.93877040T>C	GRCh38
NC_000003.11:g.93595884T>C , CM000665.1:g.93595884T>C	GRCh37
NC_000003.10:g.95078574T>C	NCBI36
NG_009813.1:g.102051A>G , LRG_572:g.102051A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1796A>G	ENSP00000330021.7:p.Asp599Gly
ENST00000394236.9:c.1796A>G MANE Select	ENSP00000377783.3:p.Asp599Gly
ENST00000407433.6:c.1751A>G	ENSP00000385794.2:p.Asp584Gly
ENST00000647936.1:c.1644+2123A>G	ENSP00000496822.1:n.1644+2123A>G
ENST00000648381.1:n.1964A>G
ENST00000648853.1:c.1754A>G	ENSP00000497262.1:p.Asp585Gly
ENST00000649585.1:c.739A>G	ENSP00000498163.1:n.739A>G
ENST00000650591.1:c.1892A>G	ENSP00000497376.1:p.Asp631Gly
ENST00000394236.7:c.1796A>G	ENSP00000377783.3:p.Asp599Gly
ENST00000407433.5:c.1403A>G	ENSP00000385794.1:p.Asp468Gly
NM_000313.3:c.1796A>G , LRG_572t1:c.1796A>G	NP_000304.2:p.Asp599Gly
NM_001314077.1:c.1892A>G , LRG_572t2:c.1892A>G	NP_001301006.1:p.Asp631Gly
NM_000313.4:c.1796A>G MANE Select	NP_000304.2:p.Asp599Gly
NM_001314077.2:c.1892A>G	NP_001301006.1:p.Asp631Gly