Canonical Allele Identifier: CA961074525
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423497_23423498insACACA , CM000676.2:g.23423497_23423498insACACA GRCh38
NC_000014.8:g.23892706_23892707insACACA , CM000676.1:g.23892706_23892707insACACA GRCh37
NC_000014.7:g.22962546_22962547insACACA NCBI36
NG_007884.1:g.17164_17165insTGTGT , LRG_384:g.17164_17165insTGTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+49_3099+50insTGTGT MANE Select ENSP00000347507.3:n.3099+49_3099+50insTGTGT
ENST00000355349.3:c.3099+49_3099+50insTGTGT ENSP00000347507.3:n.3099+49_3099+50insTGTGT
NM_000257.3:c.3099+49_3099+50insTGTGT NP_000248.2:n.3099+49_3099+50insTGTGT
XR_245686.3:n.3205+49_3205+50insTGTGT
XM_017021340.1:c.3099+49_3099+50insTGTGT XP_016876829.1:n.3099+49_3099+50insTGTGT
NM_000257.4:c.3099+49_3099+50insTGTGT MANE Select NP_000248.2:n.3099+49_3099+50insTGTGT