Canonical Allele Identifier: CA78522248

Gene: PROS1

Linked Data

• dbSNP Id: rs753516632
• gnomAD v4: 3-93879383-AAC-A
• MyVariant Identifiers: chr3:g.93598228_93598229del (hg19) ; chr3:g.93879384_93879385del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879387_93879388del , CM000665.2:g.93879387_93879388del	GRCh38
NC_000003.11:g.93598231_93598232del , CM000665.1:g.93598231_93598232del	GRCh37
NC_000003.10:g.95080921_95080922del	NCBI36
NG_009813.1:g.99706_99707del , LRG_572:g.99706_99707del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1493-71_1493-70del	ENSP00000330021.7:n.1493-71_1493-70del
ENST00000394236.9:c.1493-71_1493-70del MANE Select	ENSP00000377783.3:n.1493-71_1493-70del
ENST00000407433.6:c.1448-71_1448-70del	ENSP00000385794.2:n.1448-71_1448-70del
ENST00000647936.1:c.1493-71_1493-70del	ENSP00000496822.1:n.1493-71_1493-70del
ENST00000648381.1:n.1661-71_1661-70del
ENST00000648853.1:c.1451-71_1451-70del	ENSP00000497262.1:n.1451-71_1451-70del
ENST00000649103.1:c.1592-71_1592-70del	ENSP00000497962.1:n.1592-71_1592-70del
ENST00000649585.1:c.436-71_436-70del	ENSP00000498163.1:n.436-71_436-70del
ENST00000650591.1:c.1589-71_1589-70del	ENSP00000497376.1:n.1589-71_1589-70del
ENST00000394236.7:c.1493-71_1493-70del	ENSP00000377783.3:n.1493-71_1493-70del
ENST00000407433.5:c.1100-71_1100-70del	ENSP00000385794.1:n.1100-71_1100-70del
NM_000313.3:c.1493-71_1493-70del , LRG_572t1:c.1493-71_1493-70del	NP_000304.2:n.1493-71_1493-70del
NM_001314077.1:c.1589-71_1589-70del , LRG_572t2:c.1589-71_1589-70del	NP_001301006.1:n.1589-71_1589-70del
NM_000313.4:c.1493-71_1493-70del MANE Select	NP_000304.2:n.1493-71_1493-70del
NM_001314077.2:c.1589-71_1589-70del	NP_001301006.1:n.1589-71_1589-70del