HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32474976_32474981dup , CM000684.2:g.32474976_32474981dup | GRCh38 |
NC_000022.10:g.32870963_32870968dup , CM000684.1:g.32870963_32870968dup | GRCh37 |
NC_000022.9:g.31200963_31200968dup | NCBI36 |
NG_016001.1:g.5257_5262dup | |
NG_016001.2:g.5257_5262dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266087.12:c.-27_-22dup MANE Select | ENSP00000266087.7:n.-27_-22dup | |
ENST00000266087.11:c.-27_-22dup | ENSP00000266087.7:n.-27_-22dup | |
ENST00000420700.5:c.-27_-22dup | ENSP00000406155.1:n.-27_-22dup | |
ENST00000425028.5:c.-27_-22dup | ENSP00000395823.1:n.-27_-22dup | |
NM_012179.3:c.-27_-22dup | NP_036311.3:n.-27_-22dup | |
XM_011530106.1:c.-200_-195dup | XP_011528408.1:n.-200_-195dup | |
XM_024452207.1:c.-217_-212dup | XP_024307975.1:n.-217_-212dup | |
NM_012179.4:c.-27_-22dup MANE Select | NP_036311.3:n.-27_-22dup |