Canonical Allele Identifier: CA2123452608
Gene: MYH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431778_23431781delinsCCTT , CM000676.2:g.23431778_23431781delinsCCTT GRCh38
NC_000014.8:g.23900987_23900990delinsCCTT , CM000676.1:g.23900987_23900990delinsCCTT GRCh37
NC_000014.7:g.22970827_22970830delinsCCTT NCBI36
NG_007884.1:g.8881_8884delinsAAGG , LRG_384:g.8881_8884delinsAAGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.619_622delinsAAGG MANE Select ENSP00000347507.3:p.Lys207=
ENST00000355349.3:c.619_622delinsAAGG ENSP00000347507.3:p.Lys207=
NM_000257.3:c.619_622delinsAAGG NP_000248.2:p.Lys207=
XR_245686.3:n.725_728delinsAAGG
XM_017021340.1:c.619_622delinsAAGG XP_016876829.1:p.Lys207=
NM_000257.4:c.619_622delinsAAGG MANE Select NP_000248.2:p.Lys207=