HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173447_173448insCAC , CM000678.2:g.173447_173448insCAC | GRCh38 |
NC_000016.9:g.223446_223447insCAC , CM000678.1:g.223446_223447insCAC | GRCh37 |
NC_000016.8:g.163446_163447insCAC | NCBI36 |
NG_000006.1:g.34310_34311insCAC | |
NG_059186.1:g.1797_1798insCAC | |
NG_059271.1:g.5601_5602insCAC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251595.11:c.301-25_301-24insCAC MANE Select | ENSP00000251595.6:n.301-25_301-24insCAC | |
ENST00000251595.10:c.301-25_301-24insCAC | ENSP00000251595.6:n.301-25_301-24insCAC | |
ENST00000397806.1:c.205-25_205-24insCAC | ENSP00000380908.1:n.205-25_205-24insCAC | |
ENST00000482565.1:n.437-25_437-24insCAC | ||
ENST00000484216.1:n.387_388insCAC | ||
NM_000517.4:c.301-25_301-24insCAC | NP_000508.1:n.301-25_301-24insCAC | |
NM_000517.6:c.301-25_301-24insCAC MANE Select | NP_000508.1:n.301-25_301-24insCAC |