Canonical Allele Identifier: CA1385040026
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93900450_93900454delinsGTCTT , CM000665.2:g.93900450_93900454delinsGTCTT GRCh38
NC_000003.11:g.93619294_93619298delinsGTCTT , CM000665.1:g.93619294_93619298delinsGTCTT GRCh37
NC_000003.10:g.95101984_95101988delinsGTCTT NCBI36
NG_009813.1:g.78637_78641delinsAAGAC , LRG_572:g.78637_78641delinsAAGAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.727+350_727+354delinsAAGAC ENSP00000330021.7:n.727+350_727+354delinsAAGAC
ENST00000394236.9:c.727+350_727+354delinsAAGAC MANE Select ENSP00000377783.3:n.727+350_727+354delinsAAGAC
ENST00000407433.6:c.682+350_682+354delinsAAGAC ENSP00000385794.2:n.682+350_682+354delinsAAGAC
ENST00000647936.1:c.727+350_727+354delinsAAGAC ENSP00000496822.1:n.727+350_727+354delinsAAGAC
ENST00000648381.1:n.895+350_895+354delinsAAGAC
ENST00000648853.1:c.685+350_685+354delinsAAGAC ENSP00000497262.1:n.685+350_685+354delinsAAGAC
ENST00000649103.1:c.826+350_826+354delinsAAGAC ENSP00000497962.1:n.826+350_826+354delinsAAGAC
ENST00000650591.1:c.823+350_823+354delinsAAGAC ENSP00000497376.1:n.823+350_823+354delinsAAGAC
ENST00000394236.7:c.727+350_727+354delinsAAGAC ENSP00000377783.3:n.727+350_727+354delinsAAGAC
ENST00000407433.5:c.334+350_334+354delinsAAGAC ENSP00000385794.1:n.334+350_334+354delinsAAGAC
NM_000313.3:c.727+350_727+354delinsAAGAC , LRG_572t1:c.727+350_727+354delinsAAGAC NP_000304.2:n.727+350_727+354delinsAAGAC
NM_001314077.1:c.823+350_823+354delinsAAGAC , LRG_572t2:c.823+350_823+354delinsAAGAC NP_001301006.1:n.823+350_823+354delinsAAGAC
NM_000313.4:c.727+350_727+354delinsAAGAC MANE Select NP_000304.2:n.727+350_727+354delinsAAGAC
NM_001314077.2:c.823+350_823+354delinsAAGAC NP_001301006.1:n.823+350_823+354delinsAAGAC