HGVS | Genome Assembly |
---|---|
NC_000005.10:g.14871542_14871543insTG , CM000667.2:g.14871542_14871543insTG | GRCh38 |
NC_000005.9:g.14871651_14871652insTG , CM000667.1:g.14871651_14871652insTG | GRCh37 |
NC_000005.8:g.14924651_14924652insTG | NCBI36 |
NG_008273.1:g.5237_5238insAC | |
NG_008273.2:g.5244_5245insAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000284268.8:c.-95_-94insAC MANE Select | ENSP00000284268.6:n.-95_-94insAC | |
ENST00000284268.6:c.-95_-94insAC | ENSP00000284268.6:n.-95_-94insAC | |
ENST00000505140.1:c.-95_-94insAC | ENSP00000426332.1:n.-95_-94insAC | |
NM_054027.4:c.-95_-94insAC | NP_473368.1:n.-95_-94insAC | |
XM_011514067.1:c.-95_-94insAC | XP_011512369.1:n.-95_-94insAC | |
NM_054027.5:c.-95_-94insAC | NP_473368.1:n.-95_-94insAC | |
NM_054027.6:c.-95_-94insAC MANE Select | NP_473368.1:n.-95_-94insAC |