Canonical Allele Identifier: CA2577828221

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879378_93879383del , CM000665.2:g.93879378_93879383del	GRCh38
NC_000003.11:g.93598222_93598227del , CM000665.1:g.93598222_93598227del	GRCh37
NC_000003.10:g.95080912_95080917del	NCBI36
NG_009813.1:g.99712_99717del , LRG_572:g.99712_99717del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1493-65_1493-60del	ENSP00000330021.7:n.1493-65_1493-60del
ENST00000394236.9:c.1493-65_1493-60del MANE Select	ENSP00000377783.3:n.1493-65_1493-60del
ENST00000407433.6:c.1448-65_1448-60del	ENSP00000385794.2:n.1448-65_1448-60del
ENST00000647936.1:c.1493-65_1493-60del	ENSP00000496822.1:n.1493-65_1493-60del
ENST00000648381.1:n.1661-65_1661-60del
ENST00000648853.1:c.1451-65_1451-60del	ENSP00000497262.1:n.1451-65_1451-60del
ENST00000649103.1:c.1592-65_1592-60del	ENSP00000497962.1:n.1592-65_1592-60del
ENST00000649585.1:c.436-65_436-60del	ENSP00000498163.1:n.436-65_436-60del
ENST00000650591.1:c.1589-65_1589-60del	ENSP00000497376.1:n.1589-65_1589-60del
ENST00000394236.7:c.1493-65_1493-60del	ENSP00000377783.3:n.1493-65_1493-60del
ENST00000407433.5:c.1100-65_1100-60del	ENSP00000385794.1:n.1100-65_1100-60del
NM_000313.3:c.1493-65_1493-60del , LRG_572t1:c.1493-65_1493-60del	NP_000304.2:n.1493-65_1493-60del
NM_001314077.1:c.1589-65_1589-60del , LRG_572t2:c.1589-65_1589-60del	NP_001301006.1:n.1589-65_1589-60del
NM_000313.4:c.1493-65_1493-60del MANE Select	NP_000304.2:n.1493-65_1493-60del
NM_001314077.2:c.1589-65_1589-60del	NP_001301006.1:n.1589-65_1589-60del