Canonical Allele Identifier: CA2666654539

Gene: PROS1

Linked Data

• gnomAD v4: 3-93879336-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879336A>G , CM000665.2:g.93879336A>G	GRCh38
NC_000003.11:g.93598180A>G , CM000665.1:g.93598180A>G	GRCh37
NC_000003.10:g.95080870A>G	NCBI36
NG_009813.1:g.99755T>C , LRG_572:g.99755T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1493-22T>C	ENSP00000330021.7:n.1493-22T>C
ENST00000394236.9:c.1493-22T>C MANE Select	ENSP00000377783.3:n.1493-22T>C
ENST00000407433.6:c.1448-22T>C	ENSP00000385794.2:n.1448-22T>C
ENST00000647936.1:c.1493-22T>C	ENSP00000496822.1:n.1493-22T>C
ENST00000648381.1:n.1661-22T>C
ENST00000648853.1:c.1451-22T>C	ENSP00000497262.1:n.1451-22T>C
ENST00000649103.1:c.1592-22T>C	ENSP00000497962.1:n.1592-22T>C
ENST00000649585.1:c.436-22T>C	ENSP00000498163.1:n.436-22T>C
ENST00000650591.1:c.1589-22T>C	ENSP00000497376.1:n.1589-22T>C
ENST00000394236.7:c.1493-22T>C	ENSP00000377783.3:n.1493-22T>C
ENST00000407433.5:c.1100-22T>C	ENSP00000385794.1:n.1100-22T>C
NM_000313.3:c.1493-22T>C , LRG_572t1:c.1493-22T>C	NP_000304.2:n.1493-22T>C
NM_001314077.1:c.1589-22T>C , LRG_572t2:c.1589-22T>C	NP_001301006.1:n.1589-22T>C
NM_000313.4:c.1493-22T>C MANE Select	NP_000304.2:n.1493-22T>C
NM_001314077.2:c.1589-22T>C	NP_001301006.1:n.1589-22T>C