Canonical Allele Identifier: CA353672669

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615495T>G (hg19) ; chr3:g.93896651T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896651T>G , CM000665.2:g.93896651T>G	GRCh38
NC_000003.11:g.93615495T>G , CM000665.1:g.93615495T>G	GRCh37
NC_000003.10:g.95098185T>G	NCBI36
NG_009813.1:g.82440A>C , LRG_572:g.82440A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.890A>C	ENSP00000330021.7:p.Tyr297Ser
ENST00000394236.9:c.890A>C MANE Select	ENSP00000377783.3:p.Tyr297Ser
ENST00000407433.6:c.845A>C	ENSP00000385794.2:p.Tyr282Ser
ENST00000647936.1:c.890A>C	ENSP00000496822.1:p.Tyr297Ser
ENST00000648381.1:n.1058A>C
ENST00000648853.1:c.848A>C	ENSP00000497262.1:p.Tyr283Ser
ENST00000649103.1:c.989A>C	ENSP00000497962.1:n.989A>C
ENST00000650591.1:c.986A>C	ENSP00000497376.1:p.Tyr329Ser
ENST00000394236.7:c.890A>C	ENSP00000377783.3:p.Tyr297Ser
ENST00000407433.5:c.497A>C	ENSP00000385794.1:p.Tyr166Ser
NM_000313.3:c.890A>C , LRG_572t1:c.890A>C	NP_000304.2:p.Tyr297Ser
NM_001314077.1:c.986A>C , LRG_572t2:c.986A>C	NP_001301006.1:p.Tyr329Ser
NM_000313.4:c.890A>C MANE Select	NP_000304.2:p.Tyr297Ser
NM_001314077.2:c.986A>C	NP_001301006.1:p.Tyr329Ser