Canonical Allele Identifier: CA2123441392
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417663_23417666delinsTGCA , CM000676.2:g.23417663_23417666delinsTGCA GRCh38
NC_000014.8:g.23886872_23886875delinsTGCA , CM000676.1:g.23886872_23886875delinsTGCA GRCh37
NC_000014.7:g.22956712_22956715delinsTGCA NCBI36
NG_007884.1:g.22996_22999delinsTGCA , LRG_384:g.22996_22999delinsTGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4190_4193delinsTGCA MANE Select ENSP00000347507.3:p.Leu1397=
ENST00000355349.3:c.4190_4193delinsTGCA ENSP00000347507.3:p.Leu1397=
NM_000257.3:c.4190_4193delinsTGCA NP_000248.2:p.Leu1397=
XM_017021340.1:c.4190_4193delinsTGCA XP_016876829.1:p.Leu1397=
NM_000257.4:c.4190_4193delinsTGCA MANE Select NP_000248.2:p.Leu1397=