Canonical Allele Identifier: CA353672532

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93615433G>C (hg19) ; chr3:g.93896589G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93896589G>C , CM000665.2:g.93896589G>C	GRCh38
NC_000003.11:g.93615433G>C , CM000665.1:g.93615433G>C	GRCh37
NC_000003.10:g.95098123G>C	NCBI36
NG_009813.1:g.82502C>G , LRG_572:g.82502C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.952C>G	ENSP00000330021.7:p.Pro318Ala
ENST00000394236.9:c.952C>G MANE Select	ENSP00000377783.3:p.Pro318Ala
ENST00000407433.6:c.907C>G	ENSP00000385794.2:p.Pro303Ala
ENST00000647936.1:c.952C>G	ENSP00000496822.1:p.Pro318Ala
ENST00000648381.1:n.1120C>G
ENST00000648853.1:c.910C>G	ENSP00000497262.1:p.Pro304Ala
ENST00000649103.1:c.1051C>G	ENSP00000497962.1:n.1051C>G
ENST00000650591.1:c.1048C>G	ENSP00000497376.1:p.Pro350Ala
ENST00000394236.7:c.952C>G	ENSP00000377783.3:p.Pro318Ala
ENST00000407433.5:c.559C>G	ENSP00000385794.1:p.Pro187Ala
NM_000313.3:c.952C>G , LRG_572t1:c.952C>G	NP_000304.2:p.Pro318Ala
NM_001314077.1:c.1048C>G , LRG_572t2:c.1048C>G	NP_001301006.1:p.Pro350Ala
NM_000313.4:c.952C>G MANE Select	NP_000304.2:p.Pro318Ala
NM_001314077.2:c.1048C>G	NP_001301006.1:p.Pro350Ala