Canonical Allele Identifier: CA961071343

Gene: MYH7

Linked Data

• dbSNP Id: rs1892389110
• gnomAD v3: 14-23419710-AAAG-A
• gnomAD v4: 14-23419710-AAAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23419714_23419716del , CM000676.2:g.23419714_23419716del	GRCh38
NC_000014.8:g.23888923_23888925del , CM000676.1:g.23888923_23888925del	GRCh37
NC_000014.7:g.22958763_22958765del	NCBI36
NG_007884.1:g.20949_20951del , LRG_384:g.20949_20951del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3727-104_3727-102del MANE Select	ENSP00000347507.3:n.3727-104_3727-102del
ENST00000355349.3:c.3727-104_3727-102del	ENSP00000347507.3:n.3727-104_3727-102del
NM_000257.3:c.3727-104_3727-102del	NP_000248.2:n.3727-104_3727-102del
XM_017021340.1:c.3727-104_3727-102del	XP_016876829.1:n.3727-104_3727-102del
NM_000257.4:c.3727-104_3727-102del MANE Select	NP_000248.2:n.3727-104_3727-102del