Canonical Allele Identifier: CA353673099

Gene: PROS1

Linked Data

• gnomAD v4: 3-93900818-G-T
• MyVariant Identifiers: chr3:g.93619662G>T (hg19) ; chr3:g.93900818G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93900818G>T , CM000665.2:g.93900818G>T	GRCh38
NC_000003.11:g.93619662G>T , CM000665.1:g.93619662G>T	GRCh37
NC_000003.10:g.95102352G>T	NCBI36
NG_009813.1:g.78273C>A , LRG_572:g.78273C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.713C>A	ENSP00000330021.7:p.Ser238Ter
ENST00000394236.9:c.713C>A MANE Select	ENSP00000377783.3:p.Ser238Ter
ENST00000407433.6:c.668C>A	ENSP00000385794.2:p.Ser223Ter
ENST00000647936.1:c.713C>A	ENSP00000496822.1:p.Ser238Ter
ENST00000648381.1:n.881C>A
ENST00000648853.1:c.671C>A	ENSP00000497262.1:p.Ser224Ter
ENST00000649103.1:c.812C>A	ENSP00000497962.1:n.812C>A
ENST00000650591.1:c.809C>A	ENSP00000497376.1:p.Ser270Ter
ENST00000394236.7:c.713C>A	ENSP00000377783.3:p.Ser238Ter
ENST00000407433.5:c.320C>A	ENSP00000385794.1:p.Ser107Ter
NM_000313.3:c.713C>A , LRG_572t1:c.713C>A	NP_000304.2:p.Ser238Ter
NM_001314077.1:c.809C>A , LRG_572t2:c.809C>A	NP_001301006.1:p.Ser270Ter
NM_000313.4:c.713C>A MANE Select	NP_000304.2:p.Ser238Ter
NM_001314077.2:c.809C>A	NP_001301006.1:p.Ser270Ter