Canonical Allele Identifier: CA2624235464
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423449_23423450insTA , CM000676.2:g.23423449_23423450insTA GRCh38
NC_000014.8:g.23892658_23892659insTA , CM000676.1:g.23892658_23892659insTA GRCh37
NC_000014.7:g.22962498_22962499insTA NCBI36
NG_007884.1:g.17213_17214insAT , LRG_384:g.17213_17214insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+98_3099+99insAT MANE Select ENSP00000347507.3:n.3099+98_3099+99insAT
ENST00000355349.3:c.3099+98_3099+99insAT ENSP00000347507.3:n.3099+98_3099+99insAT
NM_000257.3:c.3099+98_3099+99insAT NP_000248.2:n.3099+98_3099+99insAT
XR_245686.3:n.3205+98_3205+99insAT
XM_017021340.1:c.3099+98_3099+99insAT XP_016876829.1:n.3099+98_3099+99insAT
NM_000257.4:c.3099+98_3099+99insAT MANE Select NP_000248.2:n.3099+98_3099+99insAT