Canonical Allele Identifier: CA2123461864
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415083_23415084delinsTT , CM000676.2:g.23415083_23415084delinsTT GRCh38
NC_000014.8:g.23884292_23884293delinsTT , CM000676.1:g.23884292_23884293delinsTT GRCh37
NC_000014.7:g.22954132_22954133delinsTT NCBI36
NG_007884.1:g.25578_25579delinsAA , LRG_384:g.25578_25579delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.5470_5471delinsAA MANE Select ENSP00000347507.3:p.Asn1824=
ENST00000355349.3:c.5470_5471delinsAA ENSP00000347507.3:p.Asn1824=
NM_000257.3:c.5470_5471delinsAA NP_000248.2:p.Asn1824=
XM_017021340.1:c.5470_5471delinsAA XP_016876829.1:p.Asn1824=
NM_000257.4:c.5470_5471delinsAA MANE Select NP_000248.2:p.Asn1824=