Canonical Allele Identifier: CA353672817

Gene: PROS1

Linked Data

• gnomAD v4: 3-93898468-G-T
• MyVariant Identifiers: chr3:g.93617312G>T (hg19) ; chr3:g.93898468G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93898468G>T , CM000665.2:g.93898468G>T	GRCh38
NC_000003.11:g.93617312G>T , CM000665.1:g.93617312G>T	GRCh37
NC_000003.10:g.95100002G>T	NCBI36
NG_009813.1:g.80623C>A , LRG_572:g.80623C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.829C>A	ENSP00000330021.7:p.Gln277Lys
ENST00000394236.9:c.829C>A MANE Select	ENSP00000377783.3:p.Gln277Lys
ENST00000407433.6:c.784C>A	ENSP00000385794.2:p.Gln262Lys
ENST00000647936.1:c.829C>A	ENSP00000496822.1:p.Gln277Lys
ENST00000648381.1:n.997C>A
ENST00000648853.1:c.787C>A	ENSP00000497262.1:p.Gln263Lys
ENST00000649103.1:c.928C>A	ENSP00000497962.1:n.928C>A
ENST00000650591.1:c.925C>A	ENSP00000497376.1:p.Gln309Lys
ENST00000394236.7:c.829C>A	ENSP00000377783.3:p.Gln277Lys
ENST00000407433.5:c.436C>A	ENSP00000385794.1:p.Gln146Lys
NM_000313.3:c.829C>A , LRG_572t1:c.829C>A	NP_000304.2:p.Gln277Lys
NM_001314077.1:c.925C>A , LRG_572t2:c.925C>A	NP_001301006.1:p.Gln309Lys
NM_000313.4:c.829C>A MANE Select	NP_000304.2:p.Gln277Lys
NM_001314077.2:c.925C>A	NP_001301006.1:p.Gln309Lys