Canonical Allele Identifier: CA2757500348

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93873779T>A , CM000665.2:g.93873779T>A	GRCh38
NC_000003.11:g.93592623T>A , CM000665.1:g.93592623T>A	GRCh37
NC_000003.10:g.95075313T>A	NCBI36
NG_009813.1:g.105312A>T , LRG_572:g.105312A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.*2-366A>T	ENSP00000330021.7:n.*2-366A>T
ENST00000394236.9:c.*466A>T MANE Select	ENSP00000377783.3:n.*466A>T
ENST00000407433.6:c.*466A>T	ENSP00000385794.2:n.*466A>T
ENST00000647936.1:c.*600A>T	ENSP00000496822.1:n.*600A>T
ENST00000648381.1:n.2665A>T
ENST00000648853.1:c.*466A>T	ENSP00000497262.1:n.*466A>T
ENST00000650591.1:c.*466A>T	ENSP00000497376.1:n.*466A>T
ENST00000394236.7:c.*466A>T	ENSP00000377783.3:n.*466A>T
ENST00000407433.5:c.*466A>T	ENSP00000385794.1:n.*466A>T
NM_000313.3:c.*466A>T , LRG_572t1:c.*466A>T	NP_000304.2:n.*466A>T
NM_001314077.1:c.*466A>T , LRG_572t2:c.*466A>T	NP_001301006.1:n.*466A>T
NM_000313.4:c.*466A>T MANE Select	NP_000304.2:n.*466A>T
NM_001314077.2:c.*466A>T	NP_001301006.1:n.*466A>T