Canonical Allele Identifier: CA353672513

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615425G>C (hg19) ; chr3:g.93896581G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896581G>C , CM000665.2:g.93896581G>C	GRCh38
NC_000003.11:g.93615425G>C , CM000665.1:g.93615425G>C	GRCh37
NC_000003.10:g.95098115G>C	NCBI36
NG_009813.1:g.82510C>G , LRG_572:g.82510C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.960C>G	ENSP00000330021.7:p.Ile320Met
ENST00000394236.9:c.960C>G MANE Select	ENSP00000377783.3:p.Ile320Met
ENST00000407433.6:c.915C>G	ENSP00000385794.2:p.Ile305Met
ENST00000647936.1:c.960C>G	ENSP00000496822.1:p.Ile320Met
ENST00000648381.1:n.1128C>G
ENST00000648853.1:c.918C>G	ENSP00000497262.1:p.Ile306Met
ENST00000649103.1:c.1059C>G	ENSP00000497962.1:n.1059C>G
ENST00000650591.1:c.1056C>G	ENSP00000497376.1:p.Ile352Met
ENST00000394236.7:c.960C>G	ENSP00000377783.3:p.Ile320Met
ENST00000407433.5:c.567C>G	ENSP00000385794.1:p.Ile189Met
NM_000313.3:c.960C>G , LRG_572t1:c.960C>G	NP_000304.2:p.Ile320Met
NM_001314077.1:c.1056C>G , LRG_572t2:c.1056C>G	NP_001301006.1:p.Ile352Met
NM_000313.4:c.960C>G MANE Select	NP_000304.2:p.Ile320Met
NM_001314077.2:c.1056C>G	NP_001301006.1:p.Ile352Met