Canonical Allele Identifier: CA353669403

Gene: PROS1

Linked Data

• gnomAD v4: 3-93874266-C-G
• MyVariant Identifiers: chr3:g.93593110C>G (hg19) ; chr3:g.93874266C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874266C>G , CM000665.2:g.93874266C>G	GRCh38
NC_000003.11:g.93593110C>G , CM000665.1:g.93593110C>G	GRCh37
NC_000003.10:g.95075800C>G	NCBI36
NG_009813.1:g.104825G>C , LRG_572:g.104825G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.2010G>C	ENSP00000330021.7:p.Trp670Cys
ENST00000394236.9:c.2010G>C MANE Select	ENSP00000377783.3:p.Trp670Cys
ENST00000407433.6:c.1965G>C	ENSP00000385794.2:p.Trp655Cys
ENST00000647936.1:c.*113G>C	ENSP00000496822.1:n.*113G>C
ENST00000648381.1:n.2178G>C
ENST00000648853.1:c.1968G>C	ENSP00000497262.1:p.Trp656Cys
ENST00000650591.1:c.2106G>C	ENSP00000497376.1:p.Trp702Cys
ENST00000394236.7:c.2010G>C	ENSP00000377783.3:p.Trp670Cys
ENST00000407433.5:c.1617G>C	ENSP00000385794.1:p.Trp539Cys
NM_000313.3:c.2010G>C , LRG_572t1:c.2010G>C	NP_000304.2:p.Trp670Cys
NM_001314077.1:c.2106G>C , LRG_572t2:c.2106G>C	NP_001301006.1:p.Trp702Cys
NM_000313.4:c.2010G>C MANE Select	NP_000304.2:p.Trp670Cys
NM_001314077.2:c.2106G>C	NP_001301006.1:p.Trp702Cys