Canonical Allele Identifier: CA1385059412
Gene: PROS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93927321_93927322delinsCA , CM000665.2:g.93927321_93927322delinsCA GRCh38
NC_000003.11:g.93646165_93646166delinsCA , CM000665.1:g.93646165_93646166delinsCA GRCh37
NC_000003.10:g.95128855_95128856delinsCA NCBI36
NG_009813.1:g.51769_51770delinsTG , LRG_572:g.51769_51770delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.162_163delinsTG ENSP00000330021.7:p.Leu54=
ENST00000394236.9:c.162_163delinsTG MANE Select ENSP00000377783.3:p.Leu54=
ENST00000407433.6:c.162_163delinsTG ENSP00000385794.2:p.Leu54=
ENST00000472684.2:c.-232_-231delinsTG ENSP00000419616.2:n.-232_-231delinsTG
ENST00000647936.1:c.162_163delinsTG ENSP00000496822.1:p.Leu54=
ENST00000648381.1:n.330_331delinsTG
ENST00000648853.1:c.120_121delinsTG ENSP00000497262.1:p.Leu40=
ENST00000649103.1:c.141_142delinsTG ENSP00000497962.1:p.Leu47=
ENST00000650591.1:c.258_259delinsTG ENSP00000497376.1:p.Leu86=
ENST00000348974.4:c.258_259delinsTG ENSP00000330021.6:p.Leu86=
ENST00000394236.7:c.162_163delinsTG ENSP00000377783.3:p.Leu54=
ENST00000407433.5:c.-232_-231delinsTG ENSP00000385794.1:n.-232_-231delinsTG
ENST00000472684.1:c.-232_-231delinsTG ENSP00000419616.1:n.-232_-231delinsTG
NM_000313.3:c.162_163delinsTG , LRG_572t1:c.162_163delinsTG NP_000304.2:p.Leu54=
NM_001314077.1:c.258_259delinsTG , LRG_572t2:c.258_259delinsTG NP_001301006.1:p.Leu86=
NM_000313.4:c.162_163delinsTG MANE Select NP_000304.2:p.Leu54=
NM_001314077.2:c.258_259delinsTG NP_001301006.1:p.Leu86=