Canonical Allele Identifier: CA2123456525
Gene: MYH7 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23434031_23434032delinsAC , CM000676.2:g.23434031_23434032delinsAC GRCh38
NC_000014.8:g.23903240_23903241delinsAC , CM000676.1:g.23903240_23903241delinsAC GRCh37
NC_000014.7:g.22973080_22973081delinsAC NCBI36
NG_007884.1:g.6630_6631delinsGT , LRG_384:g.6630_6631delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.-9+162_-9+163delinsGT MANE Select ENSP00000347507.3:n.-9+162_-9+163delinsGT
ENST00000355349.3:c.-9+162_-9+163delinsGT ENSP00000347507.3:n.-9+162_-9+163delinsGT
NM_000257.3:c.-9+162_-9+163delinsGT NP_000248.2:n.-9+162_-9+163delinsGT
XR_245686.3:n.98+162_98+163delinsGT
XM_017021340.1:c.-8-292_-8-291delinsGT XP_016876829.1:n.-8-292_-8-291delinsGT
NM_000257.4:c.-9+162_-9+163delinsGT MANE Select NP_000248.2:n.-9+162_-9+163delinsGT
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