Canonical Allele Identifier: CA353669734

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93593173C>A (hg19) ; chr3:g.93874329C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93874329C>A , CM000665.2:g.93874329C>A	GRCh38
NC_000003.11:g.93593173C>A , CM000665.1:g.93593173C>A	GRCh37
NC_000003.10:g.95075863C>A	NCBI36
NG_009813.1:g.104762G>T , LRG_572:g.104762G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1947G>T	ENSP00000330021.7:p.Leu649Phe
ENST00000394236.9:c.1947G>T MANE Select	ENSP00000377783.3:p.Leu649Phe
ENST00000407433.6:c.1902G>T	ENSP00000385794.2:p.Leu634Phe
ENST00000647936.1:c.*50G>T	ENSP00000496822.1:n.*50G>T
ENST00000648381.1:n.2115G>T
ENST00000648853.1:c.1905G>T	ENSP00000497262.1:p.Leu635Phe
ENST00000650591.1:c.2043G>T	ENSP00000497376.1:p.Leu681Phe
ENST00000394236.7:c.1947G>T	ENSP00000377783.3:p.Leu649Phe
ENST00000407433.5:c.1554G>T	ENSP00000385794.1:p.Leu518Phe
NM_000313.3:c.1947G>T , LRG_572t1:c.1947G>T	NP_000304.2:p.Leu649Phe
NM_001314077.1:c.2043G>T , LRG_572t2:c.2043G>T	NP_001301006.1:p.Leu681Phe
NM_000313.4:c.1947G>T MANE Select	NP_000304.2:p.Leu649Phe
NM_001314077.2:c.2043G>T	NP_001301006.1:p.Leu681Phe