Canonical Allele Identifier: CA1385036758

Gene: PROS1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93892862A= , CM000665.2:g.93892862A=	GRCh38
NC_000003.11:g.93611706A= , CM000665.1:g.93611706A=	GRCh37
NC_000003.10:g.95094396A=	NCBI36
NG_009813.1:g.86229T= , LRG_572:g.86229T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1155+71T=	ENSP00000330021.7:n.1155+71T=
ENST00000394236.9:c.1155+71T= MANE Select	ENSP00000377783.3:n.1155+71T=
ENST00000407433.6:c.1110+71T=	ENSP00000385794.2:n.1110+71T=
ENST00000647936.1:c.1155+71T=	ENSP00000496822.1:n.1155+71T=
ENST00000648381.1:n.1323+71T=
ENST00000648853.1:c.1113+71T=	ENSP00000497262.1:n.1113+71T=
ENST00000649103.1:c.1254+71T=	ENSP00000497962.1:n.1254+71T=
ENST00000650591.1:c.1251+71T=	ENSP00000497376.1:n.1251+71T=
ENST00000394236.7:c.1155+71T=	ENSP00000377783.3:n.1155+71T=
ENST00000407433.5:c.762+71T=	ENSP00000385794.1:n.762+71T=
NM_000313.3:c.1155+71T= , LRG_572t1:c.1155+71T=	NP_000304.2:n.1155+71T=
NM_001314077.1:c.1251+71T= , LRG_572t2:c.1251+71T=	NP_001301006.1:n.1251+71T=
NM_000313.4:c.1155+71T= MANE Select	NP_000304.2:n.1155+71T=
NM_001314077.2:c.1251+71T=	NP_001301006.1:n.1251+71T=