Canonical Allele Identifier: CA2601755926
Gene: PROS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93905522_93905524del , CM000665.2:g.93905522_93905524del GRCh38
NC_000003.11:g.93624366_93624368del , CM000665.1:g.93624366_93624368del GRCh37
NC_000003.10:g.95107056_95107058del NCBI36
NG_009813.1:g.73568_73570del , LRG_572:g.73568_73570del

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.601+261_601+263del ENSP00000330021.7:n.601+261_601+263del
ENST00000394236.9:c.601+261_601+263del MANE Select ENSP00000377783.3:n.601+261_601+263del
ENST00000407433.6:c.556+306_556+308del ENSP00000385794.2:n.556+306_556+308del
ENST00000647936.1:c.601+261_601+263del ENSP00000496822.1:n.601+261_601+263del
ENST00000648381.1:n.769+261_769+263del
ENST00000648853.1:c.559+261_559+263del ENSP00000497262.1:n.559+261_559+263del
ENST00000649103.1:c.700+261_700+263del ENSP00000497962.1:n.700+261_700+263del
ENST00000650591.1:c.697+261_697+263del ENSP00000497376.1:n.697+261_697+263del
ENST00000394236.7:c.601+261_601+263del ENSP00000377783.3:n.601+261_601+263del
ENST00000407433.5:c.208+261_208+263del ENSP00000385794.1:n.208+261_208+263del
NM_000313.3:c.601+261_601+263del , LRG_572t1:c.601+261_601+263del NP_000304.2:n.601+261_601+263del
NM_001314077.1:c.697+261_697+263del , LRG_572t2:c.697+261_697+263del NP_001301006.1:n.697+261_697+263del
NM_000313.4:c.601+261_601+263del MANE Select NP_000304.2:n.601+261_601+263del
NM_001314077.2:c.697+261_697+263del NP_001301006.1:n.697+261_697+263del