HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7530211_7530223del , CM000681.2:g.7530211_7530223del | GRCh38 |
NC_000019.9:g.7595097_7595109del , CM000681.1:g.7595097_7595109del | GRCh37 |
NC_000019.8:g.7501097_7501109del | NCBI36 |
NG_013374.1:g.1060_1072del | |
NG_015806.1:g.12602_12614del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000264079.11:c.1360-75_1360-63del MANE Select | ENSP00000264079.5:n.1360-75_1360-63del | |
ENST00000264079.10:c.1360-75_1360-63del | ENSP00000264079.5:n.1360-75_1360-63del | |
ENST00000394321.9:n.1675-75_1675-63del | ||
ENST00000594692.1:n.356-75_356-63del | ||
ENST00000595860.5:n.543-75_543-63del | ||
ENST00000599334.1:c.237-224_237-212del | ||
NM_020533.2:c.1360-75_1360-63del | NP_065394.1:n.1360-75_1360-63del | |
NM_020533.3:c.1360-75_1360-63del MANE Select | NP_065394.1:n.1360-75_1360-63del |