Canonical Allele Identifier: CA2123448366
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23420855_23420856delinsAT , CM000676.2:g.23420855_23420856delinsAT GRCh38
NC_000014.8:g.23890064_23890065delinsAT , CM000676.1:g.23890064_23890065delinsAT GRCh37
NC_000014.7:g.22959904_22959905delinsAT NCBI36
NG_007884.1:g.19806_19807delinsAT , LRG_384:g.19806_19807delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3336+102_3336+103delinsAT MANE Select ENSP00000347507.3:n.3336+102_3336+103delinsAT
ENST00000355349.3:c.3336+102_3336+103delinsAT ENSP00000347507.3:n.3336+102_3336+103delinsAT
NM_000257.3:c.3336+102_3336+103delinsAT NP_000248.2:n.3336+102_3336+103delinsAT
XR_245686.3:n.3444+102_3444+103delinsAT
XM_017021340.1:c.3336+102_3336+103delinsAT XP_016876829.1:n.3336+102_3336+103delinsAT
NM_000257.4:c.3336+102_3336+103delinsAT MANE Select NP_000248.2:n.3336+102_3336+103delinsAT