Canonical Allele Identifier: CA2123466270

Genomic Alleles

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

Transcript Alleles

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