Canonical Allele Identifier: CA704289584
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1298631264

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23421236_23421253dup , CM000676.2:g.23421236_23421253dup GRCh38
NC_000014.8:g.23890445_23890462dup , CM000676.1:g.23890445_23890462dup GRCh37
NC_000014.7:g.22960285_22960302dup NCBI36
NG_007884.1:g.19410_19427dup , LRG_384:g.19410_19427dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3246-204_3246-187dup MANE Select ENSP00000347507.3:n.3246-204_3246-187dup
ENST00000355349.3:c.3246-204_3246-187dup ENSP00000347507.3:n.3246-204_3246-187dup
NM_000257.3:c.3246-204_3246-187dup NP_000248.2:n.3246-204_3246-187dup
XR_245686.3:n.3354-204_3354-187dup
XM_017021340.1:c.3246-204_3246-187dup XP_016876829.1:n.3246-204_3246-187dup
NM_000257.4:c.3246-204_3246-187dup MANE Select NP_000248.2:n.3246-204_3246-187dup