Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232545543G>C , CM000664.2:g.232545543G>C | GRCh38 |
| NC_000002.11:g.233410253G>C , CM000664.1:g.233410253G>C | GRCh37 |
| NC_000002.10:g.233118497G>C | NCBI36 |
| NG_012954.1:g.10817G>C | |
| NG_012954.2:g.10852G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000408957.7:c.*2564C>G (TIGD1) MANE Select | ENSP00000386186.3:n.*2564C>G | |
| ENST00000651502.1:c.1381G>C (CHRNG) MANE Select | ENSP00000498757.1:p.Gly461Arg | |
| ENST00000389492.3:c.1225G>C (CHRNG) | ENSP00000374143.3:p.Gly409Arg | |
| ENST00000389494.7:c.1381G>C (CHRNG) | ENSP00000374145.3:p.Gly461Arg | |
| NM_005199.4:c.1381G>C (CHRNG) | NP_005190.4:p.Gly461Arg | |
| NM_005199.5:c.1381G>C (CHRNG) MANE Select | NP_005190.4:p.Gly461Arg | |
| NM_145702.4:c.*2564C>G (TIGD1) MANE Select | NP_663748.1:n.*2564C>G |