Canonical Allele Identifier: CA1385042398

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905437_93905438delinsCA , CM000665.2:g.93905437_93905438delinsCA	GRCh38
NC_000003.11:g.93624281_93624282delinsCA , CM000665.1:g.93624281_93624282delinsCA	GRCh37
NC_000003.10:g.95106971_95106972delinsCA	NCBI36
NG_009813.1:g.73653_73654delinsTG , LRG_572:g.73653_73654delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.601+346_601+347delinsTG	ENSP00000330021.7:n.601+346_601+347delinsTG
ENST00000394236.9:c.601+346_601+347delinsTG MANE Select	ENSP00000377783.3:n.601+346_601+347delinsTG
ENST00000407433.6:c.556+391_556+392delinsTG	ENSP00000385794.2:n.556+391_556+392delinsTG
ENST00000647936.1:c.601+346_601+347delinsTG	ENSP00000496822.1:n.601+346_601+347delinsTG
ENST00000648381.1:n.769+346_769+347delinsTG
ENST00000648853.1:c.559+346_559+347delinsTG	ENSP00000497262.1:n.559+346_559+347delinsTG
ENST00000649103.1:c.700+346_700+347delinsTG	ENSP00000497962.1:n.700+346_700+347delinsTG
ENST00000650591.1:c.697+346_697+347delinsTG	ENSP00000497376.1:n.697+346_697+347delinsTG
ENST00000394236.7:c.601+346_601+347delinsTG	ENSP00000377783.3:n.601+346_601+347delinsTG
ENST00000407433.5:c.208+346_208+347delinsTG	ENSP00000385794.1:n.208+346_208+347delinsTG
NM_000313.3:c.601+346_601+347delinsTG , LRG_572t1:c.601+346_601+347delinsTG	NP_000304.2:n.601+346_601+347delinsTG
NM_001314077.1:c.697+346_697+347delinsTG , LRG_572t2:c.697+346_697+347delinsTG	NP_001301006.1:n.697+346_697+347delinsTG
NM_000313.4:c.601+346_601+347delinsTG MANE Select	NP_000304.2:n.601+346_601+347delinsTG
NM_001314077.2:c.697+346_697+347delinsTG	NP_001301006.1:n.697+346_697+347delinsTG