Canonical Allele Identifier: CA1385026684

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873823_93873824delinsCA , CM000665.2:g.93873823_93873824delinsCA	GRCh38
NC_000003.11:g.93592667_93592668delinsCA , CM000665.1:g.93592667_93592668delinsCA	GRCh37
NC_000003.10:g.95075357_95075358delinsCA	NCBI36
NG_009813.1:g.105267_105268delinsTG , LRG_572:g.105267_105268delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*2-411_*2-410delinsTG	ENSP00000330021.7:n.*2-411_*2-410delinsTG
ENST00000394236.9:c.*421_*422delinsTG MANE Select	ENSP00000377783.3:n.*421_*422delinsTG
ENST00000407433.6:c.*421_*422delinsTG	ENSP00000385794.2:n.*421_*422delinsTG
ENST00000647936.1:c.*555_*556delinsTG	ENSP00000496822.1:n.*555_*556delinsTG
ENST00000648381.1:n.2620_2621delinsTG
ENST00000648853.1:c.*421_*422delinsTG	ENSP00000497262.1:n.*421_*422delinsTG
ENST00000650591.1:c.*421_*422delinsTG	ENSP00000497376.1:n.*421_*422delinsTG
ENST00000394236.7:c.*421_*422delinsTG	ENSP00000377783.3:n.*421_*422delinsTG
ENST00000407433.5:c.*421_*422delinsTG	ENSP00000385794.1:n.*421_*422delinsTG
NM_000313.3:c.*421_*422delinsTG , LRG_572t1:c.*421_*422delinsTG	NP_000304.2:n.*421_*422delinsTG
NM_001314077.1:c.*421_*422delinsTG , LRG_572t2:c.*421_*422delinsTG	NP_001301006.1:n.*421_*422delinsTG
NM_000313.4:c.*421_*422delinsTG MANE Select	NP_000304.2:n.*421_*422delinsTG
NM_001314077.2:c.*421_*422delinsTG	NP_001301006.1:n.*421_*422delinsTG