Canonical Allele Identifier: CA612937351
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423433_23423434insGAAACACACACACACA , CM000676.2:g.23423433_23423434insGAAACACACACACACA GRCh38
NC_000014.8:g.23892642_23892643insGAAACACACACACACA , CM000676.1:g.23892642_23892643insGAAACACACACACACA GRCh37
NC_000014.7:g.22962482_22962483insGAAACACACACACACA NCBI36
NG_007884.1:g.17231_17232insGTGTGTGTGTTTCTGT , LRG_384:g.17231_17232insGTGTGTGTGTTTCTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+116_3099+117insGTGTGTGTGTTTCTGT MANE Select ENSP00000347507.3:n.3099+116_3099+117insGTGTGTGTGTTTCTGT
ENST00000355349.3:c.3099+116_3099+117insGTGTGTGTGTTTCTGT ENSP00000347507.3:n.3099+116_3099+117insGTGTGTGTGTTTCTGT
NM_000257.3:c.3099+116_3099+117insGTGTGTGTGTTTCTGT NP_000248.2:n.3099+116_3099+117insGTGTGTGTGTTTCTGT
XR_245686.3:n.3205+116_3205+117insGTGTGTGTGTTTCTGT
XM_017021340.1:c.3099+116_3099+117insGTGTGTGTGTTTCTGT XP_016876829.1:n.3099+116_3099+117insGTGTGTGTGTTTCTGT
NM_000257.4:c.3099+116_3099+117insGTGTGTGTGTTTCTGT MANE Select NP_000248.2:n.3099+116_3099+117insGTGTGTGTGTTTCTGT