Canonical Allele Identifier: CA353672153

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598134C>A (hg19) ; chr3:g.93879290C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879290C>A , CM000665.2:g.93879290C>A	GRCh38
NC_000003.11:g.93598134C>A , CM000665.1:g.93598134C>A	GRCh37
NC_000003.10:g.95080824C>A	NCBI36
NG_009813.1:g.99801G>T , LRG_572:g.99801G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.1517G>T	ENSP00000330021.7:p.Trp506Leu
ENST00000394236.9:c.1517G>T MANE Select	ENSP00000377783.3:p.Trp506Leu
ENST00000407433.6:c.1472G>T	ENSP00000385794.2:p.Trp491Leu
ENST00000647936.1:c.1517G>T	ENSP00000496822.1:p.Trp506Leu
ENST00000648381.1:n.1685G>T
ENST00000648853.1:c.1475G>T	ENSP00000497262.1:p.Trp492Leu
ENST00000649103.1:c.1616G>T	ENSP00000497962.1:n.1616G>T
ENST00000649585.1:c.460G>T	ENSP00000498163.1:n.460G>T
ENST00000650591.1:c.1613G>T	ENSP00000497376.1:p.Trp538Leu
ENST00000394236.7:c.1517G>T	ENSP00000377783.3:p.Trp506Leu
ENST00000407433.5:c.1124G>T	ENSP00000385794.1:p.Trp375Leu
NM_000313.3:c.1517G>T , LRG_572t1:c.1517G>T	NP_000304.2:p.Trp506Leu
NM_001314077.1:c.1613G>T , LRG_572t2:c.1613G>T	NP_001301006.1:p.Trp538Leu
NM_000313.4:c.1517G>T MANE Select	NP_000304.2:p.Trp506Leu
NM_001314077.2:c.1613G>T	NP_001301006.1:p.Trp538Leu