Canonical Allele Identifier: CA2123468626

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417324_23417325delinsCG , CM000676.2:g.23417324_23417325delinsCG GRCh38
NC_000014.8:g.23886533_23886534delinsCG , CM000676.1:g.23886533_23886534delinsCG GRCh37
NC_000014.7:g.22956373_22956374delinsCG NCBI36
NG_007884.1:g.23337_23338delinsCG , LRG_384:g.23337_23338delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4354-7_4354-6delinsCG (MYH7) MANE Select ENSP00000347507.3:n.4354-7_4354-6delinsCG
ENST00000355349.3:c.4354-7_4354-6delinsCG (MYH7) ENSP00000347507.3:n.4354-7_4354-6delinsCG
NM_000257.3:c.4354-7_4354-6delinsCG (MYH7) NP_000248.2:n.4354-7_4354-6delinsCG
NR_126491.1:n.764_765delinsCG (MHRT)
XM_017021340.1:c.4354-7_4354-6delinsCG (MYH7) XP_016876829.1:n.4354-7_4354-6delinsCG
NM_000257.4:c.4354-7_4354-6delinsCG (MYH7) MANE Select NP_000248.2:n.4354-7_4354-6delinsCG