HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23416319_23416320delinsAG , CM000676.2:g.23416319_23416320delinsAG | GRCh38 |
NC_000014.8:g.23885528_23885529delinsAG , CM000676.1:g.23885528_23885529delinsAG | GRCh37 |
NC_000014.7:g.22955368_22955369delinsAG | NCBI36 |
NG_007884.1:g.24342_24343delinsCT , LRG_384:g.24342_24343delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.4645-8_4645-7delinsCT (MYH7) MANE Select | ENSP00000347507.3:n.4645-8_4645-7delinsCT | |
ENST00000355349.3:c.4645-8_4645-7delinsCT (MYH7) | ENSP00000347507.3:n.4645-8_4645-7delinsCT | |
NM_000257.3:c.4645-8_4645-7delinsCT (MYH7) | NP_000248.2:n.4645-8_4645-7delinsCT | |
NR_126491.1:n.558+22_558+23delinsAG (MHRT) | ||
XM_017021340.1:c.4645-8_4645-7delinsCT (MYH7) | XP_016876829.1:n.4645-8_4645-7delinsCT | |
NM_000257.4:c.4645-8_4645-7delinsCT (MYH7) MANE Select | NP_000248.2:n.4645-8_4645-7delinsCT |