Linked Data
dbSNP Id:
rs35045877
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.149981786dup , CM000667.2:g.149981786dup | GRCh38 |
| NC_000005.9:g.149361349dup , CM000667.1:g.149361349dup | GRCh37 |
| NC_000005.8:g.149341542dup | NCBI36 |
| NG_007147.2:g.22904dup , LRG_684:g.22904dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286298.5:c.2193dup MANE Select | ENSP00000286298.4:p.Asn732GlnfsTer6 | |
| ENST00000286298.4:c.2193dup | ENSP00000286298.4:p.Asn732GlnfsTer6 | |
| ENST00000503336.1:c.372+3435dup | ENSP00000426053.1:n.372+3435dup | |
| NM_000112.3:c.2193dup , LRG_684t1:c.2193dup | NP_000103.2:p.Asn732GlnfsTer6 | |
| XM_017009191.2:c.2193dup | XP_016864680.1:p.Asn732GlnfsTer6 | |
| NM_000112.4:c.2193dup MANE Select | NP_000103.2:p.Asn732GlnfsTer6 |