HGVS | Genome Assembly |
---|---|
NC_000016.10:g.46698020_46698021delinsCA , CM000678.2:g.46698020_46698021delinsCA | GRCh38 |
NC_000016.9:g.46731932_46731933delinsCA , CM000678.1:g.46731932_46731933delinsCA | GRCh37 |
NC_000016.8:g.45289433_45289434delinsCA | NCBI36 |
NG_028241.1:g.13375_13376delinsCA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000219097.7:c.*435_*436delinsCA MANE Select | ENSP00000219097.2:n.*435_*436delinsCA | |
ENST00000219097.6:c.*435_*436delinsCA | ENSP00000219097.2:n.*435_*436delinsCA | |
ENST00000566860.1:c.*435_*436delinsCA | ENSP00000456981.1:n.*435_*436delinsCA | |
ENST00000567000.2:n.1198_1199delinsCA | ||
NM_014321.3:c.*435_*436delinsCA | NP_055136.1:n.*435_*436delinsCA | |
NR_037620.1:n.1313_1314delinsCA | ||
NM_014321.4:c.*435_*436delinsCA MANE Select | NP_055136.1:n.*435_*436delinsCA | |
NR_037620.2:n.1300_1301delinsCA |