Canonical Allele Identifier: CA353671616

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93598006C>G (hg19) ; chr3:g.93879162C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93879162C>G , CM000665.2:g.93879162C>G	GRCh38
NC_000003.11:g.93598006C>G , CM000665.1:g.93598006C>G	GRCh37
NC_000003.10:g.95080696C>G	NCBI36
NG_009813.1:g.99929G>C , LRG_572:g.99929G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348974.5:c.1644+1G>C	ENSP00000330021.7:n.1644+1G>C
ENST00000394236.9:c.1644+1G>C MANE Select	ENSP00000377783.3:n.1644+1G>C
ENST00000407433.6:c.1599+1G>C	ENSP00000385794.2:n.1599+1G>C
ENST00000647936.1:c.1644+1G>C	ENSP00000496822.1:n.1644+1G>C
ENST00000648381.1:n.1812+1G>C
ENST00000648853.1:c.1602+1G>C	ENSP00000497262.1:n.1602+1G>C
ENST00000649103.1:c.1743+1G>C	ENSP00000497962.1:n.1743+1G>C
ENST00000649585.1:c.587+1G>C	ENSP00000498163.1:n.587+1G>C
ENST00000650591.1:c.1740+1G>C	ENSP00000497376.1:n.1740+1G>C
ENST00000394236.7:c.1644+1G>C	ENSP00000377783.3:n.1644+1G>C
ENST00000407433.5:c.1251+1G>C	ENSP00000385794.1:n.1251+1G>C
NM_000313.3:c.1644+1G>C , LRG_572t1:c.1644+1G>C	NP_000304.2:n.1644+1G>C
NM_001314077.1:c.1740+1G>C , LRG_572t2:c.1740+1G>C	NP_001301006.1:n.1740+1G>C
NM_000313.4:c.1644+1G>C MANE Select	NP_000304.2:n.1644+1G>C
NM_001314077.2:c.1740+1G>C	NP_001301006.1:n.1740+1G>C