Canonical Allele Identifier: CA2528305708
Gene: PROS1 HGNC NCBI

Linked Data

gnomAD v4: 3-93874172-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.93874172C>A , CM000665.2:g.93874172C>A GRCh38
NC_000003.11:g.93593016C>A , CM000665.1:g.93593016C>A GRCh37
NC_000003.10:g.95075706C>A NCBI36
NG_009813.1:g.104919G>T , LRG_572:g.104919G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000348974.5:c.*1+72G>T ENSP00000330021.7:n.*1+72G>T
ENST00000394236.9:c.*73G>T MANE Select ENSP00000377783.3:n.*73G>T
ENST00000407433.6:c.*73G>T ENSP00000385794.2:n.*73G>T
ENST00000647936.1:c.*207G>T ENSP00000496822.1:n.*207G>T
ENST00000648381.1:n.2272G>T
ENST00000648853.1:c.*73G>T ENSP00000497262.1:n.*73G>T
ENST00000650591.1:c.*73G>T ENSP00000497376.1:n.*73G>T
ENST00000394236.7:c.*73G>T ENSP00000377783.3:n.*73G>T
ENST00000407433.5:c.*73G>T ENSP00000385794.1:n.*73G>T
NM_000313.3:c.*73G>T , LRG_572t1:c.*73G>T NP_000304.2:n.*73G>T
NM_001314077.1:c.*73G>T , LRG_572t2:c.*73G>T NP_001301006.1:n.*73G>T
NM_000313.4:c.*73G>T MANE Select NP_000304.2:n.*73G>T
NM_001314077.2:c.*73G>T NP_001301006.1:n.*73G>T