Canonical Allele Identifier: CA2666654461

Gene: PROS1

Linked Data

• gnomAD v4: 3-93879014-TTAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879016_93879018del , CM000665.2:g.93879016_93879018del	GRCh38
NC_000003.11:g.93597860_93597862del , CM000665.1:g.93597860_93597862del	GRCh37
NC_000003.10:g.95080550_95080552del	NCBI36
NG_009813.1:g.100074_100076del , LRG_572:g.100074_100076del

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1644+146_1644+148del	ENSP00000330021.7:n.1644+146_1644+148del
ENST00000394236.9:c.1644+146_1644+148del MANE Select	ENSP00000377783.3:n.1644+146_1644+148del
ENST00000407433.6:c.1599+146_1599+148del	ENSP00000385794.2:n.1599+146_1599+148del
ENST00000647936.1:c.1644+146_1644+148del	ENSP00000496822.1:n.1644+146_1644+148del
ENST00000648381.1:n.1812+146_1812+148del
ENST00000648853.1:c.1602+146_1602+148del	ENSP00000497262.1:n.1602+146_1602+148del
ENST00000649103.1:c.1743+146_1743+148del	ENSP00000497962.1:n.1743+146_1743+148del
ENST00000649585.1:c.587+146_587+148del	ENSP00000498163.1:n.587+146_587+148del
ENST00000650591.1:c.1740+146_1740+148del	ENSP00000497376.1:n.1740+146_1740+148del
ENST00000394236.7:c.1644+146_1644+148del	ENSP00000377783.3:n.1644+146_1644+148del
ENST00000407433.5:c.1251+146_1251+148del	ENSP00000385794.1:n.1251+146_1251+148del
NM_000313.3:c.1644+146_1644+148del , LRG_572t1:c.1644+146_1644+148del	NP_000304.2:n.1644+146_1644+148del
NM_001314077.1:c.1740+146_1740+148del , LRG_572t2:c.1740+146_1740+148del	NP_001301006.1:n.1740+146_1740+148del
NM_000313.4:c.1644+146_1644+148del MANE Select	NP_000304.2:n.1644+146_1644+148del
NM_001314077.2:c.1740+146_1740+148del	NP_001301006.1:n.1740+146_1740+148del