Canonical Allele Identifier: CA1385030478
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93878888_93878890delinsTGA , CM000665.2:g.93878888_93878890delinsTGA GRCh38
NC_000003.11:g.93597732_93597734delinsTGA , CM000665.1:g.93597732_93597734delinsTGA GRCh37
NC_000003.10:g.95080422_95080424delinsTGA NCBI36
NG_009813.1:g.100201_100203delinsTCA , LRG_572:g.100201_100203delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1644+273_1644+275delinsTCA ENSP00000330021.7:n.1644+273_1644+275delinsTCA
ENST00000394236.9:c.1644+273_1644+275delinsTCA MANE Select ENSP00000377783.3:n.1644+273_1644+275delinsTCA
ENST00000407433.6:c.1599+273_1599+275delinsTCA ENSP00000385794.2:n.1599+273_1599+275delinsTCA
ENST00000647936.1:c.1644+273_1644+275delinsTCA ENSP00000496822.1:n.1644+273_1644+275delinsTCA
ENST00000648381.1:n.1812+273_1812+275delinsTCA
ENST00000648853.1:c.1602+273_1602+275delinsTCA ENSP00000497262.1:n.1602+273_1602+275delinsTCA
ENST00000649103.1:c.1743+273_1743+275delinsTCA ENSP00000497962.1:n.1743+273_1743+275delinsTCA
ENST00000649585.1:c.587+273_587+275delinsTCA ENSP00000498163.1:n.587+273_587+275delinsTCA
ENST00000650591.1:c.1740+273_1740+275delinsTCA ENSP00000497376.1:n.1740+273_1740+275delinsTCA
ENST00000394236.7:c.1644+273_1644+275delinsTCA ENSP00000377783.3:n.1644+273_1644+275delinsTCA
ENST00000407433.5:c.1251+273_1251+275delinsTCA ENSP00000385794.1:n.1251+273_1251+275delinsTCA
NM_000313.3:c.1644+273_1644+275delinsTCA , LRG_572t1:c.1644+273_1644+275delinsTCA NP_000304.2:n.1644+273_1644+275delinsTCA
NM_001314077.1:c.1740+273_1740+275delinsTCA , LRG_572t2:c.1740+273_1740+275delinsTCA NP_001301006.1:n.1740+273_1740+275delinsTCA
NM_000313.4:c.1644+273_1644+275delinsTCA MANE Select NP_000304.2:n.1644+273_1644+275delinsTCA
NM_001314077.2:c.1740+273_1740+275delinsTCA NP_001301006.1:n.1740+273_1740+275delinsTCA