Canonical Allele Identifier: CA353669535

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593135C>G (hg19) ; chr3:g.93874291C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874291C>G , CM000665.2:g.93874291C>G	GRCh38
NC_000003.11:g.93593135C>G , CM000665.1:g.93593135C>G	GRCh37
NC_000003.10:g.95075825C>G	NCBI36
NG_009813.1:g.104800G>C , LRG_572:g.104800G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1985G>C	ENSP00000330021.7:p.Arg662Thr
ENST00000394236.9:c.1985G>C MANE Select	ENSP00000377783.3:p.Arg662Thr
ENST00000407433.6:c.1940G>C	ENSP00000385794.2:p.Arg647Thr
ENST00000647936.1:c.*88G>C	ENSP00000496822.1:n.*88G>C
ENST00000648381.1:n.2153G>C
ENST00000648853.1:c.1943G>C	ENSP00000497262.1:p.Arg648Thr
ENST00000650591.1:c.2081G>C	ENSP00000497376.1:p.Arg694Thr
ENST00000394236.7:c.1985G>C	ENSP00000377783.3:p.Arg662Thr
ENST00000407433.5:c.1592G>C	ENSP00000385794.1:p.Arg531Thr
NM_000313.3:c.1985G>C , LRG_572t1:c.1985G>C	NP_000304.2:p.Arg662Thr
NM_001314077.1:c.2081G>C , LRG_572t2:c.2081G>C	NP_001301006.1:p.Arg694Thr
NM_000313.4:c.1985G>C MANE Select	NP_000304.2:p.Arg662Thr
NM_001314077.2:c.2081G>C	NP_001301006.1:p.Arg694Thr