Canonical Allele Identifier: CA353672697

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615508G>C (hg19) ; chr3:g.93896664G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896664G>C , CM000665.2:g.93896664G>C	GRCh38
NC_000003.11:g.93615508G>C , CM000665.1:g.93615508G>C	GRCh37
NC_000003.10:g.95098198G>C	NCBI36
NG_009813.1:g.82427C>G , LRG_572:g.82427C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.877C>G	ENSP00000330021.7:p.Leu293Val
ENST00000394236.9:c.877C>G MANE Select	ENSP00000377783.3:p.Leu293Val
ENST00000407433.6:c.832C>G	ENSP00000385794.2:p.Leu278Val
ENST00000647936.1:c.877C>G	ENSP00000496822.1:p.Leu293Val
ENST00000648381.1:n.1045C>G
ENST00000648853.1:c.835C>G	ENSP00000497262.1:p.Leu279Val
ENST00000649103.1:c.976C>G	ENSP00000497962.1:n.976C>G
ENST00000650591.1:c.973C>G	ENSP00000497376.1:p.Leu325Val
ENST00000394236.7:c.877C>G	ENSP00000377783.3:p.Leu293Val
ENST00000407433.5:c.484C>G	ENSP00000385794.1:p.Leu162Val
NM_000313.3:c.877C>G , LRG_572t1:c.877C>G	NP_000304.2:p.Leu293Val
NM_001314077.1:c.973C>G , LRG_572t2:c.973C>G	NP_001301006.1:p.Leu325Val
NM_000313.4:c.877C>G MANE Select	NP_000304.2:p.Leu293Val
NM_001314077.2:c.973C>G	NP_001301006.1:p.Leu325Val