Canonical Allele Identifier: CA1385026836

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874131_93874132delinsAG , CM000665.2:g.93874131_93874132delinsAG	GRCh38
NC_000003.11:g.93592975_93592976delinsAG , CM000665.1:g.93592975_93592976delinsAG	GRCh37
NC_000003.10:g.95075665_95075666delinsAG	NCBI36
NG_009813.1:g.104959_104960delinsCT , LRG_572:g.104959_104960delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+112_*1+113delinsCT	ENSP00000330021.7:n.*1+112_*1+113delinsCT
ENST00000394236.9:c.*113_*114delinsCT MANE Select	ENSP00000377783.3:n.*113_*114delinsCT
ENST00000407433.6:c.*113_*114delinsCT	ENSP00000385794.2:n.*113_*114delinsCT
ENST00000647936.1:c.*247_*248delinsCT	ENSP00000496822.1:n.*247_*248delinsCT
ENST00000648381.1:n.2312_2313delinsCT
ENST00000648853.1:c.*113_*114delinsCT	ENSP00000497262.1:n.*113_*114delinsCT
ENST00000650591.1:c.*113_*114delinsCT	ENSP00000497376.1:n.*113_*114delinsCT
ENST00000394236.7:c.*113_*114delinsCT	ENSP00000377783.3:n.*113_*114delinsCT
ENST00000407433.5:c.*113_*114delinsCT	ENSP00000385794.1:n.*113_*114delinsCT
NM_000313.3:c.*113_*114delinsCT , LRG_572t1:c.*113_*114delinsCT	NP_000304.2:n.*113_*114delinsCT
NM_001314077.1:c.*113_*114delinsCT , LRG_572t2:c.*113_*114delinsCT	NP_001301006.1:n.*113_*114delinsCT
NM_000313.4:c.*113_*114delinsCT MANE Select	NP_000304.2:n.*113_*114delinsCT
NM_001314077.2:c.*113_*114delinsCT	NP_001301006.1:n.*113_*114delinsCT