Canonical Allele Identifier: CA2624231002
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23419723_23419724insCCTTCCC , CM000676.2:g.23419723_23419724insCCTTCCC GRCh38
NC_000014.8:g.23888932_23888933insCCTTCCC , CM000676.1:g.23888932_23888933insCCTTCCC GRCh37
NC_000014.7:g.22958772_22958773insCCTTCCC NCBI36
NG_007884.1:g.20938_20939insGGGAAGG , LRG_384:g.20938_20939insGGGAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3727-115_3727-114insGGGAAGG MANE Select ENSP00000347507.3:n.3727-115_3727-114insGGGAAGG
ENST00000355349.3:c.3727-115_3727-114insGGGAAGG ENSP00000347507.3:n.3727-115_3727-114insGGGAAGG
NM_000257.3:c.3727-115_3727-114insGGGAAGG NP_000248.2:n.3727-115_3727-114insGGGAAGG
XM_017021340.1:c.3727-115_3727-114insGGGAAGG XP_016876829.1:n.3727-115_3727-114insGGGAAGG
NM_000257.4:c.3727-115_3727-114insGGGAAGG MANE Select NP_000248.2:n.3727-115_3727-114insGGGAAGG