Canonical Allele Identifier: CA353672146

Gene: PROS1

Linked Data

• gnomAD v4: 3-93879288-G-C
• MyVariant Identifiers: chr3:g.93598132G>C (hg19) ; chr3:g.93879288G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879288G>C , CM000665.2:g.93879288G>C	GRCh38
NC_000003.11:g.93598132G>C , CM000665.1:g.93598132G>C	GRCh37
NC_000003.10:g.95080822G>C	NCBI36
NG_009813.1:g.99803C>G , LRG_572:g.99803C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1519C>G	ENSP00000330021.7:p.His507Asp
ENST00000394236.9:c.1519C>G MANE Select	ENSP00000377783.3:p.His507Asp
ENST00000407433.6:c.1474C>G	ENSP00000385794.2:p.His492Asp
ENST00000647936.1:c.1519C>G	ENSP00000496822.1:p.His507Asp
ENST00000648381.1:n.1687C>G
ENST00000648853.1:c.1477C>G	ENSP00000497262.1:p.His493Asp
ENST00000649103.1:c.1618C>G	ENSP00000497962.1:n.1618C>G
ENST00000649585.1:c.462C>G	ENSP00000498163.1:n.462C>G
ENST00000650591.1:c.1615C>G	ENSP00000497376.1:p.His539Asp
ENST00000394236.7:c.1519C>G	ENSP00000377783.3:p.His507Asp
ENST00000407433.5:c.1126C>G	ENSP00000385794.1:p.His376Asp
NM_000313.3:c.1519C>G , LRG_572t1:c.1519C>G	NP_000304.2:p.His507Asp
NM_001314077.1:c.1615C>G , LRG_572t2:c.1615C>G	NP_001301006.1:p.His539Asp
NM_000313.4:c.1519C>G MANE Select	NP_000304.2:p.His507Asp
NM_001314077.2:c.1615C>G	NP_001301006.1:p.His539Asp