Canonical Allele Identifier: CA1385042410
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93905461_93905463delinsTGG , CM000665.2:g.93905461_93905463delinsTGG GRCh38
NC_000003.11:g.93624305_93624307delinsTGG , CM000665.1:g.93624305_93624307delinsTGG GRCh37
NC_000003.10:g.95106995_95106997delinsTGG NCBI36
NG_009813.1:g.73628_73630delinsCCA , LRG_572:g.73628_73630delinsCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.601+321_601+323delinsCCA ENSP00000330021.7:n.601+321_601+323delinsCCA
ENST00000394236.9:c.601+321_601+323delinsCCA MANE Select ENSP00000377783.3:n.601+321_601+323delinsCCA
ENST00000407433.6:c.556+366_556+368delinsCCA ENSP00000385794.2:n.556+366_556+368delinsCCA
ENST00000647936.1:c.601+321_601+323delinsCCA ENSP00000496822.1:n.601+321_601+323delinsCCA
ENST00000648381.1:n.769+321_769+323delinsCCA
ENST00000648853.1:c.559+321_559+323delinsCCA ENSP00000497262.1:n.559+321_559+323delinsCCA
ENST00000649103.1:c.700+321_700+323delinsCCA ENSP00000497962.1:n.700+321_700+323delinsCCA
ENST00000650591.1:c.697+321_697+323delinsCCA ENSP00000497376.1:n.697+321_697+323delinsCCA
ENST00000394236.7:c.601+321_601+323delinsCCA ENSP00000377783.3:n.601+321_601+323delinsCCA
ENST00000407433.5:c.208+321_208+323delinsCCA ENSP00000385794.1:n.208+321_208+323delinsCCA
NM_000313.3:c.601+321_601+323delinsCCA , LRG_572t1:c.601+321_601+323delinsCCA NP_000304.2:n.601+321_601+323delinsCCA
NM_001314077.1:c.697+321_697+323delinsCCA , LRG_572t2:c.697+321_697+323delinsCCA NP_001301006.1:n.697+321_697+323delinsCCA
NM_000313.4:c.601+321_601+323delinsCCA MANE Select NP_000304.2:n.601+321_601+323delinsCCA
NM_001314077.2:c.697+321_697+323delinsCCA NP_001301006.1:n.697+321_697+323delinsCCA