Canonical Allele Identifier: CA353674750

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93646252C>A (hg19) ; chr3:g.93927408C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93927408C>A , CM000665.2:g.93927408C>A	GRCh38
NC_000003.11:g.93646252C>A , CM000665.1:g.93646252C>A	GRCh37
NC_000003.10:g.95128942C>A	NCBI36
NG_009813.1:g.51683G>T , LRG_572:g.51683G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.77-1G>T	ENSP00000330021.7:n.77-1G>T
ENST00000394236.9:c.77-1G>T MANE Select	ENSP00000377783.3:n.77-1G>T
ENST00000407433.6:c.77-1G>T	ENSP00000385794.2:n.77-1G>T
ENST00000472684.2:c.-317-1G>T	ENSP00000419616.2:n.-317-1G>T
ENST00000647936.1:c.77-1G>T	ENSP00000496822.1:n.77-1G>T
ENST00000648381.1:n.245-1G>T
ENST00000648853.1:c.35-1G>T	ENSP00000497262.1:n.35-1G>T
ENST00000649103.1:c.56-1G>T	ENSP00000497962.1:n.56-1G>T
ENST00000650591.1:c.173-1G>T	ENSP00000497376.1:n.173-1G>T
ENST00000348974.4:c.173-1G>T	ENSP00000330021.6:n.173-1G>T
ENST00000394236.7:c.77-1G>T	ENSP00000377783.3:n.77-1G>T
ENST00000407433.5:c.-317-1G>T	ENSP00000385794.1:n.-317-1G>T
ENST00000472684.1:c.-317-1G>T	ENSP00000419616.1:n.-317-1G>T
NM_000313.3:c.77-1G>T , LRG_572t1:c.77-1G>T	NP_000304.2:n.77-1G>T
NM_001314077.1:c.173-1G>T , LRG_572t2:c.173-1G>T	NP_001301006.1:n.173-1G>T
NM_000313.4:c.77-1G>T MANE Select	NP_000304.2:n.77-1G>T
NM_001314077.2:c.173-1G>T	NP_001301006.1:n.173-1G>T