Canonical Allele Identifier: CA544749282

Gene: PROS1

Linked Data

• dbSNP Id: rs1354065508
• gnomAD v2: 3-93611723-T-TTATAA
• gnomAD v3: 3-93892879-T-TTATAA
• gnomAD v4: 3-93892879-T-TTATAA
• MyVariant Identifiers: chr3:g.93611723_93611724insTATAA (hg19) ; chr3:g.93892879_93892880insTATAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93892880_93892881insATAAT , CM000665.2:g.93892880_93892881insATAAT	GRCh38
NC_000003.11:g.93611724_93611725insATAAT , CM000665.1:g.93611724_93611725insATAAT	GRCh37
NC_000003.10:g.95094414_95094415insATAAT	NCBI36
NG_009813.1:g.86211_86212insTTATA , LRG_572:g.86211_86212insTTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1155+53_1155+54insTTATA	ENSP00000330021.7:n.1155+53_1155+54insTTATA
ENST00000394236.9:c.1155+53_1155+54insTTATA MANE Select	ENSP00000377783.3:n.1155+53_1155+54insTTATA
ENST00000407433.6:c.1110+53_1110+54insTTATA	ENSP00000385794.2:n.1110+53_1110+54insTTATA
ENST00000647936.1:c.1155+53_1155+54insTTATA	ENSP00000496822.1:n.1155+53_1155+54insTTATA
ENST00000648381.1:n.1323+53_1323+54insTTATA
ENST00000648853.1:c.1113+53_1113+54insTTATA	ENSP00000497262.1:n.1113+53_1113+54insTTATA
ENST00000649103.1:c.1254+53_1254+54insTTATA	ENSP00000497962.1:n.1254+53_1254+54insTTATA
ENST00000650591.1:c.1251+53_1251+54insTTATA	ENSP00000497376.1:n.1251+53_1251+54insTTATA
ENST00000394236.7:c.1155+53_1155+54insTTATA	ENSP00000377783.3:n.1155+53_1155+54insTTATA
ENST00000407433.5:c.762+53_762+54insTTATA	ENSP00000385794.1:n.762+53_762+54insTTATA
NM_000313.3:c.1155+53_1155+54insTTATA , LRG_572t1:c.1155+53_1155+54insTTATA	NP_000304.2:n.1155+53_1155+54insTTATA
NM_001314077.1:c.1251+53_1251+54insTTATA , LRG_572t2:c.1251+53_1251+54insTTATA	NP_001301006.1:n.1251+53_1251+54insTTATA
NM_000313.4:c.1155+53_1155+54insTTATA MANE Select	NP_000304.2:n.1155+53_1155+54insTTATA
NM_001314077.2:c.1251+53_1251+54insTTATA	NP_001301006.1:n.1251+53_1251+54insTTATA