HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47333255_47333256delinsTG , CM000673.2:g.47333255_47333256delinsTG | GRCh38 |
NC_000011.9:g.47354806_47354807delinsTG , CM000673.1:g.47354806_47354807delinsTG | GRCh37 |
NC_000011.8:g.47311382_47311383delinsTG | NCBI36 |
NG_007667.1:g.24447_24448delinsCA , LRG_386:g.24447_24448delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000545968.6:c.3268_3269delinsCA MANE Select | ENSP00000442795.1:p.Gln1090= | |
ENST00000256993.8:c.3268_3269delinsCA | ENSP00000256993.5:p.Gln1090= | |
ENST00000399249.6:c.3268_3269delinsCA | ENSP00000382193.2:p.Gln1090= | |
ENST00000545968.5:c.3268_3269delinsCA | ENSP00000442795.1:p.Gln1090= | |
NM_000256.3:c.3268_3269delinsCA , LRG_386t1:c.3268_3269delinsCA MANE Select | NP_000247.2:p.Gln1090= | |
XM_011520117.1:c.3250_3251delinsCA | XP_011518419.1:p.Gln1084= | |
XM_011520118.1:c.3187_3188delinsCA | XP_011518420.1:p.Gln1063= |