Canonical Allele Identifier: CA353672309

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93611884G>C (hg19) ; chr3:g.93893040G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893040G>C , CM000665.2:g.93893040G>C	GRCh38
NC_000003.11:g.93611884G>C , CM000665.1:g.93611884G>C	GRCh37
NC_000003.10:g.95094574G>C	NCBI36
NG_009813.1:g.86051C>G , LRG_572:g.86051C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1048C>G	ENSP00000330021.7:p.Leu350Val
ENST00000394236.9:c.1048C>G MANE Select	ENSP00000377783.3:p.Leu350Val
ENST00000407433.6:c.1003C>G	ENSP00000385794.2:p.Leu335Val
ENST00000647936.1:c.1048C>G	ENSP00000496822.1:p.Leu350Val
ENST00000648381.1:n.1216C>G
ENST00000648853.1:c.1006C>G	ENSP00000497262.1:p.Leu336Val
ENST00000649103.1:c.1147C>G	ENSP00000497962.1:n.1147C>G
ENST00000650591.1:c.1144C>G	ENSP00000497376.1:p.Leu382Val
ENST00000394236.7:c.1048C>G	ENSP00000377783.3:p.Leu350Val
ENST00000407433.5:c.655C>G	ENSP00000385794.1:p.Leu219Val
NM_000313.3:c.1048C>G , LRG_572t1:c.1048C>G	NP_000304.2:p.Leu350Val
NM_001314077.1:c.1144C>G , LRG_572t2:c.1144C>G	NP_001301006.1:p.Leu382Val
NM_000313.4:c.1048C>G MANE Select	NP_000304.2:p.Leu350Val
NM_001314077.2:c.1144C>G	NP_001301006.1:p.Leu382Val