Canonical Allele Identifier: CA1385030534

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879037_93879041delinsCCAAA , CM000665.2:g.93879037_93879041delinsCCAAA	GRCh38
NC_000003.11:g.93597881_93597885delinsCCAAA , CM000665.1:g.93597881_93597885delinsCCAAA	GRCh37
NC_000003.10:g.95080571_95080575delinsCCAAA	NCBI36
NG_009813.1:g.100050_100054delinsTTTGG , LRG_572:g.100050_100054delinsTTTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1644+122_1644+126delinsTTTGG	ENSP00000330021.7:n.1644+122_1644+126delinsTTTGG
ENST00000394236.9:c.1644+122_1644+126delinsTTTGG MANE Select	ENSP00000377783.3:n.1644+122_1644+126delinsTTTGG
ENST00000407433.6:c.1599+122_1599+126delinsTTTGG	ENSP00000385794.2:n.1599+122_1599+126delinsTTTGG
ENST00000647936.1:c.1644+122_1644+126delinsTTTGG	ENSP00000496822.1:n.1644+122_1644+126delinsTTTGG
ENST00000648381.1:n.1812+122_1812+126delinsTTTGG
ENST00000648853.1:c.1602+122_1602+126delinsTTTGG	ENSP00000497262.1:n.1602+122_1602+126delinsTTTGG
ENST00000649103.1:c.1743+122_1743+126delinsTTTGG	ENSP00000497962.1:n.1743+122_1743+126delinsTTTGG
ENST00000649585.1:c.587+122_587+126delinsTTTGG	ENSP00000498163.1:n.587+122_587+126delinsTTTGG
ENST00000650591.1:c.1740+122_1740+126delinsTTTGG	ENSP00000497376.1:n.1740+122_1740+126delinsTTTGG
ENST00000394236.7:c.1644+122_1644+126delinsTTTGG	ENSP00000377783.3:n.1644+122_1644+126delinsTTTGG
ENST00000407433.5:c.1251+122_1251+126delinsTTTGG	ENSP00000385794.1:n.1251+122_1251+126delinsTTTGG
NM_000313.3:c.1644+122_1644+126delinsTTTGG , LRG_572t1:c.1644+122_1644+126delinsTTTGG	NP_000304.2:n.1644+122_1644+126delinsTTTGG
NM_001314077.1:c.1740+122_1740+126delinsTTTGG , LRG_572t2:c.1740+122_1740+126delinsTTTGG	NP_001301006.1:n.1740+122_1740+126delinsTTTGG
NM_000313.4:c.1644+122_1644+126delinsTTTGG MANE Select	NP_000304.2:n.1644+122_1644+126delinsTTTGG
NM_001314077.2:c.1740+122_1740+126delinsTTTGG	NP_001301006.1:n.1740+122_1740+126delinsTTTGG