Canonical Allele Identifier: CA353672315

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93611886C>G (hg19) ; chr3:g.93893042C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893042C>G , CM000665.2:g.93893042C>G	GRCh38
NC_000003.11:g.93611886C>G , CM000665.1:g.93611886C>G	GRCh37
NC_000003.10:g.95094576C>G	NCBI36
NG_009813.1:g.86049G>C , LRG_572:g.86049G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1046G>C	ENSP00000330021.7:p.Trp349Ser
ENST00000394236.9:c.1046G>C MANE Select	ENSP00000377783.3:p.Trp349Ser
ENST00000407433.6:c.1001G>C	ENSP00000385794.2:p.Trp334Ser
ENST00000647936.1:c.1046G>C	ENSP00000496822.1:p.Trp349Ser
ENST00000648381.1:n.1214G>C
ENST00000648853.1:c.1004G>C	ENSP00000497262.1:p.Trp335Ser
ENST00000649103.1:c.1145G>C	ENSP00000497962.1:n.1145G>C
ENST00000650591.1:c.1142G>C	ENSP00000497376.1:p.Trp381Ser
ENST00000394236.7:c.1046G>C	ENSP00000377783.3:p.Trp349Ser
ENST00000407433.5:c.653G>C	ENSP00000385794.1:p.Trp218Ser
NM_000313.3:c.1046G>C , LRG_572t1:c.1046G>C	NP_000304.2:p.Trp349Ser
NM_001314077.1:c.1142G>C , LRG_572t2:c.1142G>C	NP_001301006.1:p.Trp381Ser
NM_000313.4:c.1046G>C MANE Select	NP_000304.2:p.Trp349Ser
NM_001314077.2:c.1142G>C	NP_001301006.1:p.Trp381Ser