HGVS | Genome Assembly |
---|---|
NC_000002.12:g.202377446_202377447insTAC , CM000664.2:g.202377446_202377447insTAC | GRCh38 |
NC_000002.11:g.203242169_203242170insTAC , CM000664.1:g.203242169_203242170insTAC | GRCh37 |
NC_000002.10:g.202950414_202950415insTAC | NCBI36 |
NG_009363.1:g.6120_6121insTAC , LRG_712:g.6120_6121insTAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374580.10:c.-29_-28insTAC MANE Select | ENSP00000363708.4:n.-29_-28insTAC | |
ENST00000374574.2:c.-29_-28insTAC | ENSP00000363702.2:n.-29_-28insTAC | |
ENST00000374580.8:c.-29_-28insTAC | ENSP00000363708.4:n.-29_-28insTAC | |
NM_001204.6:c.-29_-28insTAC , LRG_712t1:c.-29_-28insTAC | NP_001195.2:n.-29_-28insTAC | |
XM_011511687.1:c.-29_-28insTAC | XP_011509989.1:n.-29_-28insTAC | |
XM_011511688.1:c.-29_-28insTAC | XP_011509990.1:n.-29_-28insTAC | |
NM_001204.7:c.-29_-28insTAC MANE Select | NP_001195.2:n.-29_-28insTAC |