Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.6713618_6713619insG , CM000681.2:g.6713618_6713619insG | GRCh38 |
| NC_000019.9:g.6713629_6713630insG , CM000681.1:g.6713629_6713630insG | GRCh37 |
| NC_000019.8:g.6664629_6664630insG | NCBI36 |
| NG_009557.1:g.12033_12034insC , LRG_27:g.12033_12034insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695652.1:c.651-110_651-109insC | ENSP00000512083.1:n.651-110_651-109insC | |
| ENST00000245907.11:c.774-110_774-109insC MANE Select | ENSP00000245907.4:n.774-110_774-109insC | |
| ENST00000245907.10:c.774-110_774-109insC | ENSP00000245907.4:n.774-110_774-109insC | |
| ENST00000595577.1:n.278-110_278-109insC | ||
| ENST00000597442.5:n.24-110_24-109insC | ||
| NM_000064.3:c.774-110_774-109insC | NP_000055.2:n.774-110_774-109insC | |
| NM_000064.4:c.774-110_774-109insC MANE Select | NP_000055.2:n.774-110_774-109insC |