HGVS | Genome Assembly |
---|---|
NC_000012.12:g.57739481_57739483del , CM000674.2:g.57739481_57739483del | GRCh38 |
NC_000012.11:g.58133264_58133266del , CM000674.1:g.58133264_58133266del | GRCh37 |
NC_000012.10:g.56419531_56419533del | NCBI36 |
NG_029755.1:g.7681_7683del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000257897.7:c.160+2431_160+2433del (AGAP2) | ENSP00000257897.3:n.160+2431_160+2433del | |
ENST00000553221.5:n.189+1280_189+1282del (TSPAN31) | ||
NM_014770.3:c.160+2431_160+2433del (AGAP2) | NP_055585.1:n.160+2431_160+2433del | |
XM_005268626.1:c.160+2431_160+2433del (AGAP2) | XP_005268683.1:n.160+2431_160+2433del | |
XM_005268626.2:c.160+2431_160+2433del (AGAP2) | XP_005268683.1:n.160+2431_160+2433del | |
NM_014770.4:c.160+2431_160+2433del (AGAP2) | NP_055585.1:n.160+2431_160+2433del |