Canonical Allele Identifier: CA353672492

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93611968T>C (hg19) ; chr3:g.93893124T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93893124T>C , CM000665.2:g.93893124T>C	GRCh38
NC_000003.11:g.93611968T>C , CM000665.1:g.93611968T>C	GRCh37
NC_000003.10:g.95094658T>C	NCBI36
NG_009813.1:g.85967A>G , LRG_572:g.85967A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.966-2A>G	ENSP00000330021.7:n.966-2A>G
ENST00000394236.9:c.966-2A>G MANE Select	ENSP00000377783.3:n.966-2A>G
ENST00000407433.6:c.921-2A>G	ENSP00000385794.2:n.921-2A>G
ENST00000647936.1:c.966-2A>G	ENSP00000496822.1:n.966-2A>G
ENST00000648381.1:n.1134-2A>G
ENST00000648853.1:c.924-2A>G	ENSP00000497262.1:n.924-2A>G
ENST00000649103.1:c.1065-2A>G	ENSP00000497962.1:n.1065-2A>G
ENST00000650591.1:c.1062-2A>G	ENSP00000497376.1:n.1062-2A>G
ENST00000394236.7:c.966-2A>G	ENSP00000377783.3:n.966-2A>G
ENST00000407433.5:c.573-2A>G	ENSP00000385794.1:n.573-2A>G
NM_000313.3:c.966-2A>G , LRG_572t1:c.966-2A>G	NP_000304.2:n.966-2A>G
NM_001314077.1:c.1062-2A>G , LRG_572t2:c.1062-2A>G	NP_001301006.1:n.1062-2A>G
NM_000313.4:c.966-2A>G MANE Select	NP_000304.2:n.966-2A>G
NM_001314077.2:c.1062-2A>G	NP_001301006.1:n.1062-2A>G