Canonical Allele Identifier: CA2123469498

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417568_23417571delinsCCAT , CM000676.2:g.23417568_23417571delinsCCAT GRCh38
NC_000014.8:g.23886777_23886780delinsCCAT , CM000676.1:g.23886777_23886780delinsCCAT GRCh37
NC_000014.7:g.22956617_22956620delinsCCAT NCBI36
NG_007884.1:g.23091_23094delinsATGG , LRG_384:g.23091_23094delinsATGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4285_4288delinsATGG (MYH7) MANE Select ENSP00000347507.3:p.Met1429=
ENST00000355349.3:c.4285_4288delinsATGG (MYH7) ENSP00000347507.3:p.Met1429=
NM_000257.3:c.4285_4288delinsATGG (MYH7) NP_000248.2:p.Met1429=
NR_126491.1:n.849_852delinsCCAT (MHRT)
XM_017021340.1:c.4285_4288delinsATGG (MYH7) XP_016876829.1:p.Met1429=
NM_000257.4:c.4285_4288delinsATGG (MYH7) MANE Select NP_000248.2:p.Met1429=