Canonical Allele Identifier: CA2547226882
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417704dup , CM000676.2:g.23417704dup GRCh38
NC_000014.8:g.23886913dup , CM000676.1:g.23886913dup GRCh37
NC_000014.7:g.22956753dup NCBI36
NG_007884.1:g.22959dup , LRG_384:g.22959dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4170-17dup MANE Select ENSP00000347507.3:n.4170-17dup
ENST00000355349.3:c.4170-17dup ENSP00000347507.3:n.4170-17dup
NM_000257.3:c.4170-17dup NP_000248.2:n.4170-17dup
XM_017021340.1:c.4170-17dup XP_016876829.1:n.4170-17dup
NM_000257.4:c.4170-17dup MANE Select NP_000248.2:n.4170-17dup