Canonical Allele Identifier: CA353669540

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593137A>C (hg19) ; chr3:g.93874293A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874293A>C , CM000665.2:g.93874293A>C	GRCh38
NC_000003.11:g.93593137A>C , CM000665.1:g.93593137A>C	GRCh37
NC_000003.10:g.95075827A>C	NCBI36
NG_009813.1:g.104798T>G , LRG_572:g.104798T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1983T>G	ENSP00000330021.7:p.Ile661Met
ENST00000394236.9:c.1983T>G MANE Select	ENSP00000377783.3:p.Ile661Met
ENST00000407433.6:c.1938T>G	ENSP00000385794.2:p.Ile646Met
ENST00000647936.1:c.*86T>G	ENSP00000496822.1:n.*86T>G
ENST00000648381.1:n.2151T>G
ENST00000648853.1:c.1941T>G	ENSP00000497262.1:p.Ile647Met
ENST00000650591.1:c.2079T>G	ENSP00000497376.1:p.Ile693Met
ENST00000394236.7:c.1983T>G	ENSP00000377783.3:p.Ile661Met
ENST00000407433.5:c.1590T>G	ENSP00000385794.1:p.Ile530Met
NM_000313.3:c.1983T>G , LRG_572t1:c.1983T>G	NP_000304.2:p.Ile661Met
NM_001314077.1:c.2079T>G , LRG_572t2:c.2079T>G	NP_001301006.1:p.Ile693Met
NM_000313.4:c.1983T>G MANE Select	NP_000304.2:p.Ile661Met
NM_001314077.2:c.2079T>G	NP_001301006.1:p.Ile693Met