Canonical Allele Identifier: CA353674703

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646231A>G (hg19) ; chr3:g.93927387A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927387A>G , CM000665.2:g.93927387A>G	GRCh38
NC_000003.11:g.93646231A>G , CM000665.1:g.93646231A>G	GRCh37
NC_000003.10:g.95128921A>G	NCBI36
NG_009813.1:g.51704T>C , LRG_572:g.51704T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.97T>C	ENSP00000330021.7:p.Ser33Pro
ENST00000394236.9:c.97T>C MANE Select	ENSP00000377783.3:p.Ser33Pro
ENST00000407433.6:c.97T>C	ENSP00000385794.2:p.Ser33Pro
ENST00000472684.2:c.-297T>C	ENSP00000419616.2:n.-297T>C
ENST00000647936.1:c.97T>C	ENSP00000496822.1:p.Ser33Pro
ENST00000648381.1:n.265T>C
ENST00000648853.1:c.55T>C	ENSP00000497262.1:p.Ser19Pro
ENST00000649103.1:c.76T>C	ENSP00000497962.1:p.Ser26Pro
ENST00000650591.1:c.193T>C	ENSP00000497376.1:p.Ser65Pro
ENST00000348974.4:c.193T>C	ENSP00000330021.6:p.Ser65Pro
ENST00000394236.7:c.97T>C	ENSP00000377783.3:p.Ser33Pro
ENST00000407433.5:c.-297T>C	ENSP00000385794.1:n.-297T>C
ENST00000472684.1:c.-297T>C	ENSP00000419616.1:n.-297T>C
NM_000313.3:c.97T>C , LRG_572t1:c.97T>C	NP_000304.2:p.Ser33Pro
NM_001314077.1:c.193T>C , LRG_572t2:c.193T>C	NP_001301006.1:p.Ser65Pro
NM_000313.4:c.97T>C MANE Select	NP_000304.2:p.Ser33Pro
NM_001314077.2:c.193T>C	NP_001301006.1:p.Ser65Pro