Canonical Allele Identifier: CA2624235414
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423441_23423442insAA , CM000676.2:g.23423441_23423442insAA GRCh38
NC_000014.8:g.23892650_23892651insAA , CM000676.1:g.23892650_23892651insAA GRCh37
NC_000014.7:g.22962490_22962491insAA NCBI36
NG_007884.1:g.17221_17222insTT , LRG_384:g.17221_17222insTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+106_3099+107insTT MANE Select ENSP00000347507.3:n.3099+106_3099+107insTT
ENST00000355349.3:c.3099+106_3099+107insTT ENSP00000347507.3:n.3099+106_3099+107insTT
NM_000257.3:c.3099+106_3099+107insTT NP_000248.2:n.3099+106_3099+107insTT
XR_245686.3:n.3205+106_3205+107insTT
XM_017021340.1:c.3099+106_3099+107insTT XP_016876829.1:n.3099+106_3099+107insTT
NM_000257.4:c.3099+106_3099+107insTT MANE Select NP_000248.2:n.3099+106_3099+107insTT