Canonical Allele Identifier: CA1385028890
Gene: PROS1 HGNC NCBI

Linked Data

dbSNP Id: rs1708199443

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93877009_93877011dup , CM000665.2:g.93877009_93877011dup GRCh38
NC_000003.11:g.93595853_93595855dup , CM000665.1:g.93595853_93595855dup GRCh37
NC_000003.10:g.95078543_95078545dup NCBI36
NG_009813.1:g.102080_102082dup , LRG_572:g.102080_102082dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000348974.5:c.1825_1827dup ENSP00000330021.7:p.Lys609_Ala610insLys
ENST00000394236.9:c.1825_1827dup MANE Select ENSP00000377783.3:p.Lys609_Ala610insLys
ENST00000407433.6:c.1780_1782dup ENSP00000385794.2:p.Lys594_Ala595insLys
ENST00000647936.1:c.1644+2152_1644+2154dup ENSP00000496822.1:n.1644+2152_1644+2154dup
ENST00000648381.1:n.1993_1995dup
ENST00000648853.1:c.1783_1785dup ENSP00000497262.1:p.Lys595_Ala596insLys
ENST00000649585.1:c.768_770dup ENSP00000498163.1:n.768_770dup
ENST00000650591.1:c.1921_1923dup ENSP00000497376.1:p.Lys641_Ala642insLys
ENST00000394236.7:c.1825_1827dup ENSP00000377783.3:p.Lys609_Ala610insLys
ENST00000407433.5:c.1432_1434dup ENSP00000385794.1:p.Lys478_Ala479insLys
NM_000313.3:c.1825_1827dup , LRG_572t1:c.1825_1827dup NP_000304.2:p.Lys609_Ala610insLys
NM_001314077.1:c.1921_1923dup , LRG_572t2:c.1921_1923dup NP_001301006.1:p.Lys641_Ala642insLys
NM_000313.4:c.1825_1827dup MANE Select NP_000304.2:p.Lys609_Ala610insLys
NM_001314077.2:c.1921_1923dup NP_001301006.1:p.Lys641_Ala642insLys