HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23424321_23424322insAGTT , CM000676.2:g.23424321_23424322insAGTT | GRCh38 |
NC_000014.8:g.23893530_23893531insAGTT , CM000676.1:g.23893530_23893531insAGTT | GRCh37 |
NC_000014.7:g.22963370_22963371insAGTT | NCBI36 |
NG_007884.1:g.16340_16341insAACT , LRG_384:g.16340_16341insAACT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.2680-173_2680-172insAACT MANE Select | ENSP00000347507.3:n.2680-173_2680-172insAACT | |
ENST00000355349.3:c.2680-173_2680-172insAACT | ENSP00000347507.3:n.2680-173_2680-172insAACT | |
NM_000257.3:c.2680-173_2680-172insAACT | NP_000248.2:n.2680-173_2680-172insAACT | |
XR_245686.3:n.2786-173_2786-172insAACT | ||
XM_017021340.1:c.2680-173_2680-172insAACT | XP_016876829.1:n.2680-173_2680-172insAACT | |
NM_000257.4:c.2680-173_2680-172insAACT MANE Select | NP_000248.2:n.2680-173_2680-172insAACT |