ClinGen Evidence Repository:
Classification
Likely Pathogenic
Condition
antithrombin III deficiency
VCEP
Thrombosis VCEP
Revel Score:
ENST00000367698 (MANE Select)
0.778
ENST00000351522
0.778
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.173903978C>T , CM000663.2:g.173903978C>T | GRCh38 |
| NC_000001.10:g.173873116C>T , CM000663.1:g.173873116C>T | GRCh37 |
| NC_000001.9:g.172139739C>T | NCBI36 |
| NG_012462.1:g.18401G>A , LRG_577:g.18401G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367698.4:c.1306G>A MANE Select | ENSP00000356671.3:p.Ala436Thr | |
| ENST00000367698.3:c.1306G>A | ENSP00000356671.3:p.Ala436Thr | |
| ENST00000617423.4:c.691G>A | ENSP00000478688.1:p.Ala231Thr | |
| NM_000488.3:c.1306G>A , LRG_577t1:c.1306G>A | NP_000479.1:p.Ala436Thr | |
| XM_005245198.2:c.1162G>A | XP_005245255.1:p.Ala388Thr | |
| NM_001365052.1:c.1162G>A | NP_001351981.1:p.Ala388Thr | |
| NM_000488.4:c.1306G>A MANE Select | NP_000479.1:p.Ala436Thr | |
| NM_001365052.2:c.1162G>A | NP_001351981.1:p.Ala388Thr | |
| NM_001386302.1:c.1429G>A | NP_001373231.1:p.Ala477Thr | |
| NM_001386303.1:c.1387G>A | NP_001373232.1:p.Ala463Thr | |
| NM_001386304.1:c.1285G>A | NP_001373233.1:p.Ala429Thr | |
| NM_001386305.1:c.1249G>A | NP_001373234.1:p.Ala417Thr | |
| NM_001386306.1:c.1090G>A | NP_001373235.1:p.Ala364Thr |