HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23417571_23417573dup , CM000676.2:g.23417571_23417573dup | GRCh38 |
NC_000014.8:g.23886780_23886782dup , CM000676.1:g.23886780_23886782dup | GRCh37 |
NC_000014.7:g.22956620_22956622dup | NCBI36 |
NG_007884.1:g.23091_23093dup , LRG_384:g.23091_23093dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.4285_4287dup (MYH7) MANE Select | ENSP00000347507.3:p.Met1429_Val1430insMet | |
ENST00000355349.3:c.4285_4287dup (MYH7) | ENSP00000347507.3:p.Met1429_Val1430insMet | |
NM_000257.3:c.4285_4287dup (MYH7) | NP_000248.2:p.Met1429_Val1430insMet | |
NR_126491.1:n.852_854dup (MHRT) | ||
XM_017021340.1:c.4285_4287dup (MYH7) | XP_016876829.1:p.Met1429_Val1430insMet | |
NM_000257.4:c.4285_4287dup (MYH7) MANE Select | NP_000248.2:p.Met1429_Val1430insMet |