Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.94429341G>C , CM000669.2:g.94429341G>C | GRCh38 |
| NC_000007.13:g.94058653G>C , CM000669.1:g.94058653G>C | GRCh37 |
| NC_000007.12:g.93896589G>C | NCBI36 |
| NG_007405.1:g.39781G>C , LRG_2:g.39781G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000089.4:c.3865G>C MANE Select | NP_000080.2:p.Ala1289Pro |
| ENST00000297268.11:c.3865G>C MANE Select | ENSP00000297268.6:p.Ala1289Pro |
| NM_000089.3:c.3865G>C , LRG_2t1:c.3865G>C | NP_000080.2:p.Ala1289Pro |
| ENST00000297268.10:c.3865G>C | ENSP00000297268.6:p.Ala1289Pro |
| ENST00000464916.1:n.913G>C | |
| ENST00000481570.5:n.4646G>C | |
| ENST00000620463.1:c.3859G>C | ENSP00000477719.1:p.Ala1287Pro |