Canonical Allele Identifier: CA2123468864

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417390_23417391delinsGC , CM000676.2:g.23417390_23417391delinsGC GRCh38
NC_000014.8:g.23886599_23886600delinsGC , CM000676.1:g.23886599_23886600delinsGC GRCh37
NC_000014.7:g.22956439_22956440delinsGC NCBI36
NG_007884.1:g.23271_23272delinsGC , LRG_384:g.23271_23272delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4354-73_4354-72delinsGC (MYH7) MANE Select ENSP00000347507.3:n.4354-73_4354-72delinsGC
ENST00000355349.3:c.4354-73_4354-72delinsGC (MYH7) ENSP00000347507.3:n.4354-73_4354-72delinsGC
NM_000257.3:c.4354-73_4354-72delinsGC (MYH7) NP_000248.2:n.4354-73_4354-72delinsGC
NR_126491.1:n.813+17_813+18delinsGC (MHRT)
XM_017021340.1:c.4354-73_4354-72delinsGC (MYH7) XP_016876829.1:n.4354-73_4354-72delinsGC
NM_000257.4:c.4354-73_4354-72delinsGC (MYH7) MANE Select NP_000248.2:n.4354-73_4354-72delinsGC