Canonical Allele Identifier: CA353672096

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598115C>G (hg19) ; chr3:g.93879271C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879271C>G , CM000665.2:g.93879271C>G	GRCh38
NC_000003.11:g.93598115C>G , CM000665.1:g.93598115C>G	GRCh37
NC_000003.10:g.95080805C>G	NCBI36
NG_009813.1:g.99820G>C , LRG_572:g.99820G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1536G>C	ENSP00000330021.7:p.Leu512Phe
ENST00000394236.9:c.1536G>C MANE Select	ENSP00000377783.3:p.Leu512Phe
ENST00000407433.6:c.1491G>C	ENSP00000385794.2:p.Leu497Phe
ENST00000647936.1:c.1536G>C	ENSP00000496822.1:p.Leu512Phe
ENST00000648381.1:n.1704G>C
ENST00000648853.1:c.1494G>C	ENSP00000497262.1:p.Leu498Phe
ENST00000649103.1:c.1635G>C	ENSP00000497962.1:n.1635G>C
ENST00000649585.1:c.479G>C	ENSP00000498163.1:n.479G>C
ENST00000650591.1:c.1632G>C	ENSP00000497376.1:p.Leu544Phe
ENST00000394236.7:c.1536G>C	ENSP00000377783.3:p.Leu512Phe
ENST00000407433.5:c.1143G>C	ENSP00000385794.1:p.Leu381Phe
NM_000313.3:c.1536G>C , LRG_572t1:c.1536G>C	NP_000304.2:p.Leu512Phe
NM_001314077.1:c.1632G>C , LRG_572t2:c.1632G>C	NP_001301006.1:p.Leu544Phe
NM_000313.4:c.1536G>C MANE Select	NP_000304.2:p.Leu512Phe
NM_001314077.2:c.1632G>C	NP_001301006.1:p.Leu544Phe