Canonical Allele Identifier: CA2123453914
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423930_23423933delinsCCTT , CM000676.2:g.23423930_23423933delinsCCTT GRCh38
NC_000014.8:g.23893139_23893142delinsCCTT , CM000676.1:g.23893139_23893142delinsCCTT GRCh37
NC_000014.7:g.22962979_22962982delinsCCTT NCBI36
NG_007884.1:g.16729_16732delinsAAGG , LRG_384:g.16729_16732delinsAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.2896_2899delinsAAGG MANE Select ENSP00000347507.3:p.Lys966=
ENST00000355349.3:c.2896_2899delinsAAGG ENSP00000347507.3:p.Lys966=
NM_000257.3:c.2896_2899delinsAAGG NP_000248.2:p.Lys966=
XR_245686.3:n.3002_3005delinsAAGG
XM_017021340.1:c.2896_2899delinsAAGG XP_016876829.1:p.Lys966=
NM_000257.4:c.2896_2899delinsAAGG MANE Select NP_000248.2:p.Lys966=