Canonical Allele Identifier: CA353673234
Gene: PROS1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93900879T>A , CM000665.2:g.93900879T>A GRCh38
NC_000003.11:g.93619723T>A , CM000665.1:g.93619723T>A GRCh37
NC_000003.10:g.95102413T>A NCBI36
NG_009813.1:g.78212A>T , LRG_572:g.78212A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.652A>T ENSP00000330021.7:p.Lys218Ter
ENST00000394236.9:c.652A>T MANE Select ENSP00000377783.3:p.Lys218Ter
ENST00000407433.6:c.607A>T ENSP00000385794.2:p.Lys203Ter
ENST00000647936.1:c.652A>T ENSP00000496822.1:p.Lys218Ter
ENST00000648381.1:n.820A>T
ENST00000648853.1:c.610A>T ENSP00000497262.1:p.Lys204Ter
ENST00000649103.1:c.751A>T ENSP00000497962.1:n.751A>T
ENST00000650591.1:c.748A>T ENSP00000497376.1:p.Lys250Ter
ENST00000394236.7:c.652A>T ENSP00000377783.3:p.Lys218Ter
ENST00000407433.5:c.259A>T ENSP00000385794.1:p.Lys87Ter
NM_000313.3:c.652A>T , LRG_572t1:c.652A>T NP_000304.2:p.Lys218Ter
NM_001314077.1:c.748A>T , LRG_572t2:c.748A>T NP_001301006.1:p.Lys250Ter
NM_000313.4:c.652A>T MANE Select NP_000304.2:p.Lys218Ter
NM_001314077.2:c.748A>T NP_001301006.1:p.Lys250Ter