Canonical Allele Identifier: CA434463041

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93595838T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93876994T>C , CM000665.2:g.93876994T>C	GRCh38
NC_000003.11:g.93595838T>C , CM000665.1:g.93595838T>C	GRCh37
NC_000003.10:g.95078528T>C	NCBI36
NG_009813.1:g.102097A>G , LRG_572:g.102097A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1842A>G	ENSP00000330021.7:p.Lys614=
ENST00000394236.9:c.1842A>G MANE Select	ENSP00000377783.3:p.Lys614=
ENST00000407433.6:c.1797A>G	ENSP00000385794.2:p.Lys599=
ENST00000647936.1:c.1644+2169A>G	ENSP00000496822.1:n.1644+2169A>G
ENST00000648381.1:n.2010A>G
ENST00000648853.1:c.1800A>G	ENSP00000497262.1:p.Lys600=
ENST00000650591.1:c.1938A>G	ENSP00000497376.1:p.Lys646=
ENST00000394236.7:c.1842A>G	ENSP00000377783.3:p.Lys614=
ENST00000407433.5:c.1449A>G	ENSP00000385794.1:p.Lys483=
NM_000313.3:c.1842A>G , LRG_572t1:c.1842A>G	NP_000304.2:p.Lys614=
NM_001314077.1:c.1938A>G , LRG_572t2:c.1938A>G	NP_001301006.1:p.Lys646=
NM_000313.4:c.1842A>G MANE Select	NP_000304.2:p.Lys614=
NM_001314077.2:c.1938A>G	NP_001301006.1:p.Lys646=