Canonical Allele Identifier: CA915948851
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 650845
ClinVar RCV Id: RCV000806076
dbSNP Id: rs1595089639

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431782_23431784del , CM000676.2:g.23431782_23431784del GRCh38
NC_000014.8:g.23900991_23900993del , CM000676.1:g.23900991_23900993del GRCh37
NC_000014.7:g.22970831_22970833del NCBI36
NG_007884.1:g.8881_8883del , LRG_384:g.8881_8883del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.619_621del MANE Select ENSP00000347507.3:p.Lys207del
ENST00000355349.3:c.619_621del ENSP00000347507.3:p.Lys207del
NM_000257.3:c.619_621del NP_000248.2:p.Lys207del
XR_245686.3:n.725_727del
XM_017021340.1:c.619_621del XP_016876829.1:p.Lys207del
NM_000257.4:c.619_621del MANE Select NP_000248.2:p.Lys207del