Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232544436G>A , CM000664.2:g.232544436G>A | GRCh38 |
| NC_000002.11:g.233409146G>A , CM000664.1:g.233409146G>A | GRCh37 |
| NC_000002.10:g.233117390G>A | NCBI36 |
| NG_012954.1:g.9710G>A | |
| NG_012954.2:g.9745G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000408957.7:c.*3671C>T (TIGD1) MANE Select | ENSP00000386186.3:n.*3671C>T | |
| ENST00000651502.1:c.1105G>A (CHRNG) MANE Select | ENSP00000498757.1:p.Asp369Asn | |
| ENST00000389492.3:c.949G>A (CHRNG) | ENSP00000374143.3:p.Asp317Asn | |
| ENST00000389494.7:c.1105G>A (CHRNG) | ENSP00000374145.3:p.Asp369Asn | |
| NM_005199.4:c.1105G>A (CHRNG) | NP_005190.4:p.Asp369Asn | |
| NM_005199.5:c.1105G>A (CHRNG) MANE Select | NP_005190.4:p.Asp369Asn | |
| NM_145702.4:c.*3671C>T (TIGD1) MANE Select | NP_663748.1:n.*3671C>T |