Canonical Allele Identifier: CA2757501283

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896502A>G , CM000665.2:g.93896502A>G	GRCh38
NC_000003.11:g.93615346A>G , CM000665.1:g.93615346A>G	GRCh37
NC_000003.10:g.95098036A>G	NCBI36
NG_009813.1:g.82589T>C , LRG_572:g.82589T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.965+74T>C	ENSP00000330021.7:n.965+74T>C
ENST00000394236.9:c.965+74T>C MANE Select	ENSP00000377783.3:n.965+74T>C
ENST00000407433.6:c.920+74T>C	ENSP00000385794.2:n.920+74T>C
ENST00000647936.1:c.965+74T>C	ENSP00000496822.1:n.965+74T>C
ENST00000648381.1:n.1133+74T>C
ENST00000648853.1:c.923+74T>C	ENSP00000497262.1:n.923+74T>C
ENST00000649103.1:c.1064+74T>C	ENSP00000497962.1:n.1064+74T>C
ENST00000650591.1:c.1061+74T>C	ENSP00000497376.1:n.1061+74T>C
ENST00000394236.7:c.965+74T>C	ENSP00000377783.3:n.965+74T>C
ENST00000407433.5:c.572+74T>C	ENSP00000385794.1:n.572+74T>C
NM_000313.3:c.965+74T>C , LRG_572t1:c.965+74T>C	NP_000304.2:n.965+74T>C
NM_001314077.1:c.1061+74T>C , LRG_572t2:c.1061+74T>C	NP_001301006.1:n.1061+74T>C
NM_000313.4:c.965+74T>C MANE Select	NP_000304.2:n.965+74T>C
NM_001314077.2:c.1061+74T>C	NP_001301006.1:n.1061+74T>C