Canonical Allele Identifier: CA2123445728
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419686_23419691delinsGAGAAA , CM000676.2:g.23419686_23419691delinsGAGAAA GRCh38
NC_000014.8:g.23888895_23888900delinsGAGAAA , CM000676.1:g.23888895_23888900delinsGAGAAA GRCh37
NC_000014.7:g.22958735_22958740delinsGAGAAA NCBI36
NG_007884.1:g.20971_20976delinsTTTCTC , LRG_384:g.20971_20976delinsTTTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3727-82_3727-77delinsTTTCTC MANE Select ENSP00000347507.3:n.3727-82_3727-77delinsTTTCTC
ENST00000355349.3:c.3727-82_3727-77delinsTTTCTC ENSP00000347507.3:n.3727-82_3727-77delinsTTTCTC
NM_000257.3:c.3727-82_3727-77delinsTTTCTC NP_000248.2:n.3727-82_3727-77delinsTTTCTC
XM_017021340.1:c.3727-82_3727-77delinsTTTCTC XP_016876829.1:n.3727-82_3727-77delinsTTTCTC
NM_000257.4:c.3727-82_3727-77delinsTTTCTC MANE Select NP_000248.2:n.3727-82_3727-77delinsTTTCTC