Canonical Allele Identifier: CA2123452721

Gene: MYH7

Linked Data

• dbSNP Id: rs1263745197

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423435_23423436insCACACACACACA , CM000676.2:g.23423435_23423436insCACACACACACA	GRCh38
NC_000014.8:g.23892644_23892645insCACACACACACA , CM000676.1:g.23892644_23892645insCACACACACACA	GRCh37
NC_000014.7:g.22962484_22962485insCACACACACACA	NCBI36
NG_007884.1:g.17231_17232insGTGTGTGTGTGT , LRG_384:g.17231_17232insGTGTGTGTGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+116_3099+117insGTGTGTGTGTGT MANE Select	ENSP00000347507.3:n.3099+116_3099+117insGTGTGTGTGTGT
ENST00000355349.3:c.3099+116_3099+117insGTGTGTGTGTGT	ENSP00000347507.3:n.3099+116_3099+117insGTGTGTGTGTGT
NM_000257.3:c.3099+116_3099+117insGTGTGTGTGTGT	NP_000248.2:n.3099+116_3099+117insGTGTGTGTGTGT
XR_245686.3:n.3205+116_3205+117insGTGTGTGTGTGT
XM_017021340.1:c.3099+116_3099+117insGTGTGTGTGTGT	XP_016876829.1:n.3099+116_3099+117insGTGTGTGTGTGT
NM_000257.4:c.3099+116_3099+117insGTGTGTGTGTGT MANE Select	NP_000248.2:n.3099+116_3099+117insGTGTGTGTGTGT