Canonical Allele Identifier: CA353673393

Gene: PROS1

Linked Data

• MyVariant Identifiers: chr3:g.93624641C>G (hg19) ; chr3:g.93905797C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.93905797C>G , CM000665.2:g.93905797C>G	GRCh38
NC_000003.11:g.93624641C>G , CM000665.1:g.93624641C>G	GRCh37
NC_000003.10:g.95107331C>G	NCBI36
NG_009813.1:g.73294G>C , LRG_572:g.73294G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000348974.5:c.588G>C	ENSP00000330021.7:p.Lys196Asn
ENST00000394236.9:c.588G>C MANE Select	ENSP00000377783.3:p.Lys196Asn
ENST00000407433.6:c.556+32G>C	ENSP00000385794.2:n.556+32G>C
ENST00000647936.1:c.588G>C	ENSP00000496822.1:p.Lys196Asn
ENST00000648381.1:n.756G>C
ENST00000648853.1:c.546G>C	ENSP00000497262.1:p.Lys182Asn
ENST00000649103.1:c.687G>C	ENSP00000497962.1:n.687G>C
ENST00000650591.1:c.684G>C	ENSP00000497376.1:p.Lys228Asn
ENST00000348974.4:c.684G>C	ENSP00000330021.6:p.Lys228Asn
ENST00000394236.7:c.588G>C	ENSP00000377783.3:p.Lys196Asn
ENST00000407433.5:c.195G>C	ENSP00000385794.1:p.Lys65Asn
NM_000313.3:c.588G>C , LRG_572t1:c.588G>C	NP_000304.2:p.Lys196Asn
NM_001314077.1:c.684G>C , LRG_572t2:c.684G>C	NP_001301006.1:p.Lys228Asn
NM_000313.4:c.588G>C MANE Select	NP_000304.2:p.Lys196Asn
NM_001314077.2:c.684G>C	NP_001301006.1:p.Lys228Asn