Canonical Allele Identifier: CA2666656907

Gene: PROS1

Linked Data

• gnomAD v4: 3-93892844-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93892844T>G , CM000665.2:g.93892844T>G	GRCh38
NC_000003.11:g.93611688T>G , CM000665.1:g.93611688T>G	GRCh37
NC_000003.10:g.95094378T>G	NCBI36
NG_009813.1:g.86247A>C , LRG_572:g.86247A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1155+89A>C	ENSP00000330021.7:n.1155+89A>C
ENST00000394236.9:c.1155+89A>C MANE Select	ENSP00000377783.3:n.1155+89A>C
ENST00000407433.6:c.1110+89A>C	ENSP00000385794.2:n.1110+89A>C
ENST00000647936.1:c.1155+89A>C	ENSP00000496822.1:n.1155+89A>C
ENST00000648381.1:n.1323+89A>C
ENST00000648853.1:c.1113+89A>C	ENSP00000497262.1:n.1113+89A>C
ENST00000649103.1:c.1254+89A>C	ENSP00000497962.1:n.1254+89A>C
ENST00000650591.1:c.1251+89A>C	ENSP00000497376.1:n.1251+89A>C
ENST00000394236.7:c.1155+89A>C	ENSP00000377783.3:n.1155+89A>C
ENST00000407433.5:c.762+89A>C	ENSP00000385794.1:n.762+89A>C
NM_000313.3:c.1155+89A>C , LRG_572t1:c.1155+89A>C	NP_000304.2:n.1155+89A>C
NM_001314077.1:c.1251+89A>C , LRG_572t2:c.1251+89A>C	NP_001301006.1:n.1251+89A>C
NM_000313.4:c.1155+89A>C MANE Select	NP_000304.2:n.1155+89A>C
NM_001314077.2:c.1251+89A>C	NP_001301006.1:n.1251+89A>C