Canonical Allele Identifier: CA353670913

Gene: PROS1

Linked Data

• dbSNP Id: rs1354833303
• MyVariant Identifiers: chr3:g.93595857T>G (hg19) ; chr3:g.93877013T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93877013T>G , CM000665.2:g.93877013T>G	GRCh38
NC_000003.11:g.93595857T>G , CM000665.1:g.93595857T>G	GRCh37
NC_000003.10:g.95078547T>G	NCBI36
NG_009813.1:g.102078A>C , LRG_572:g.102078A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1823A>C	ENSP00000330021.7:p.Asp608Ala
ENST00000394236.9:c.1823A>C MANE Select	ENSP00000377783.3:p.Asp608Ala
ENST00000407433.6:c.1778A>C	ENSP00000385794.2:p.Asp593Ala
ENST00000647936.1:c.1644+2150A>C	ENSP00000496822.1:n.1644+2150A>C
ENST00000648381.1:n.1991A>C
ENST00000648853.1:c.1781A>C	ENSP00000497262.1:p.Asp594Ala
ENST00000649585.1:c.766A>C	ENSP00000498163.1:n.766A>C
ENST00000650591.1:c.1919A>C	ENSP00000497376.1:p.Asp640Ala
ENST00000394236.7:c.1823A>C	ENSP00000377783.3:p.Asp608Ala
ENST00000407433.5:c.1430A>C	ENSP00000385794.1:p.Asp477Ala
NM_000313.3:c.1823A>C , LRG_572t1:c.1823A>C	NP_000304.2:p.Asp608Ala
NM_001314077.1:c.1919A>C , LRG_572t2:c.1919A>C	NP_001301006.1:p.Asp640Ala
NM_000313.4:c.1823A>C MANE Select	NP_000304.2:p.Asp608Ala
NM_001314077.2:c.1919A>C	NP_001301006.1:p.Asp640Ala