HGVS | Genome Assembly |
---|---|
NC_000010.11:g.94849855_94849856delinsAC , CM000672.2:g.94849855_94849856delinsAC | GRCh38 |
NC_000010.10:g.96609612_96609613delinsAC , CM000672.1:g.96609612_96609613delinsAC | GRCh37 |
NC_000010.9:g.96599602_96599603delinsAC | NCBI36 |
NG_008384.2:g.92150_92151delinsAC | |
NG_008384.3:g.92175_92176delinsAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000371321.9:c.1150-62_1150-61delinsAC MANE Select | ENSP00000360372.3:n.1150-62_1150-61delinsAC | |
ENST00000645461.1:n.2061-62_2061-61delinsAC | ||
ENST00000371321.7:c.1150-62_1150-61delinsAC | ENSP00000360372.3:n.1150-62_1150-61delinsAC | |
ENST00000464755.1:c.1913-62_1913-61delinsAC | ENSP00000483243.1:n.1913-62_1913-61delinsAC | |
NM_000769.2:c.1150-62_1150-61delinsAC | NP_000760.1:n.1150-62_1150-61delinsAC | |
NM_000769.4:c.1150-62_1150-61delinsAC MANE Select | NP_000760.1:n.1150-62_1150-61delinsAC |