Canonical Allele Identifier: CA353672508

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615423C>G (hg19) ; chr3:g.93896579C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896579C>G , CM000665.2:g.93896579C>G	GRCh38
NC_000003.11:g.93615423C>G , CM000665.1:g.93615423C>G	GRCh37
NC_000003.10:g.95098113C>G	NCBI36
NG_009813.1:g.82512G>C , LRG_572:g.82512G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.962G>C	ENSP00000330021.7:p.Ser321Thr
ENST00000394236.9:c.962G>C MANE Select	ENSP00000377783.3:p.Ser321Thr
ENST00000407433.6:c.917G>C	ENSP00000385794.2:p.Ser306Thr
ENST00000647936.1:c.962G>C	ENSP00000496822.1:p.Ser321Thr
ENST00000648381.1:n.1130G>C
ENST00000648853.1:c.920G>C	ENSP00000497262.1:p.Ser307Thr
ENST00000649103.1:c.1061G>C	ENSP00000497962.1:n.1061G>C
ENST00000650591.1:c.1058G>C	ENSP00000497376.1:p.Ser353Thr
ENST00000394236.7:c.962G>C	ENSP00000377783.3:p.Ser321Thr
ENST00000407433.5:c.569G>C	ENSP00000385794.1:p.Ser190Thr
NM_000313.3:c.962G>C , LRG_572t1:c.962G>C	NP_000304.2:p.Ser321Thr
NM_001314077.1:c.1058G>C , LRG_572t2:c.1058G>C	NP_001301006.1:p.Ser353Thr
NM_000313.4:c.962G>C MANE Select	NP_000304.2:p.Ser321Thr
NM_001314077.2:c.1058G>C	NP_001301006.1:p.Ser353Thr