Canonical Allele Identifier: CA2507033696

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873994_93873995insCA , CM000665.2:g.93873994_93873995insCA	GRCh38
NC_000003.11:g.93592838_93592839insCA , CM000665.1:g.93592838_93592839insCA	GRCh37
NC_000003.10:g.95075528_95075529insCA	NCBI36
NG_009813.1:g.105096_105097insTG , LRG_572:g.105096_105097insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*1+249_*1+250insTG	ENSP00000330021.7:n.*1+249_*1+250insTG
ENST00000394236.9:c.*250_*251insTG MANE Select	ENSP00000377783.3:n.*250_*251insTG
ENST00000407433.6:c.*250_*251insTG	ENSP00000385794.2:n.*250_*251insTG
ENST00000647936.1:c.*384_*385insTG	ENSP00000496822.1:n.*384_*385insTG
ENST00000648381.1:n.2449_2450insTG
ENST00000648853.1:c.*250_*251insTG	ENSP00000497262.1:n.*250_*251insTG
ENST00000650591.1:c.*250_*251insTG	ENSP00000497376.1:n.*250_*251insTG
ENST00000394236.7:c.*250_*251insTG	ENSP00000377783.3:n.*250_*251insTG
ENST00000407433.5:c.*250_*251insTG	ENSP00000385794.1:n.*250_*251insTG
NM_000313.3:c.*250_*251insTG , LRG_572t1:c.*250_*251insTG	NP_000304.2:n.*250_*251insTG
NM_001314077.1:c.*250_*251insTG , LRG_572t2:c.*250_*251insTG	NP_001301006.1:n.*250_*251insTG
NM_000313.4:c.*250_*251insTG MANE Select	NP_000304.2:n.*250_*251insTG
NM_001314077.2:c.*250_*251insTG	NP_001301006.1:n.*250_*251insTG