Linked Data
gnomAD v2:
5-161275150-G-GGTAAA
MyVariant Identifiers:
chr5:g.161275150_161275151insGTAAA (hg19)
chr5:g.161848144_161848145insGTAAA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.161848145_161848146insTAAAG , CM000667.2:g.161848145_161848146insTAAAG | GRCh38 |
| NC_000005.9:g.161275151_161275152insTAAAG , CM000667.1:g.161275151_161275152insTAAAG | GRCh37 |
| NC_000005.8:g.161207729_161207730insTAAAG | NCBI36 |
| NG_011548.1:g.5955_5956insTAAAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393943.10:c.-293_-292insTAAAG MANE Select | ENSP00000377517.4:n.-293_-292insTAAAG | |
| ENST00000635916.2:n.483_484insTAAAG | ||
| ENST00000638112.1:c.-247-46_-247-45insTAAAG | ENSP00000489839.1:n.-247-46_-247-45insTAAAG | |
| ENST00000023897.10:c.-247-46_-247-45insTAAAG | ENSP00000023897.6:n.-247-46_-247-45insTAAAG | |
| ENST00000393943.9:c.-293_-292insTAAAG | ENSP00000377517.4:n.-293_-292insTAAAG | |
| ENST00000428797.7:c.-247-46_-247-45insTAAAG | ENSP00000393097.2:n.-247-46_-247-45insTAAAG | |
| ENST00000635096.1:c.-247-46_-247-45insTAAAG | ENSP00000489033.1:n.-247-46_-247-45insTAAAG | |
| NM_000806.5:c.-247-46_-247-45insTAAAG | NP_000797.2:n.-247-46_-247-45insTAAAG | |
| NM_001127643.1:c.-247-46_-247-45insTAAAG | NP_001121115.1:n.-247-46_-247-45insTAAAG | |
| NM_001127644.1:c.-293_-292insTAAAG | NP_001121116.1:n.-293_-292insTAAAG | |
| XR_941158.3:n.89+2375_89+2376insTTTAC | ||
| NM_001127644.2:c.-293_-292insTAAAG MANE Select | NP_001121116.1:n.-293_-292insTAAAG | |
| NM_001127643.2:c.-247-46_-247-45insTAAAG | NP_001121115.1:n.-247-46_-247-45insTAAAG |