Canonical Allele Identifier: CA2624238920

Gene: MYH7

Linked Data

• gnomAD v4: 14-23417798-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23417800del , CM000676.2:g.23417800del	GRCh38
NC_000014.8:g.23887009del , CM000676.1:g.23887009del	GRCh37
NC_000014.7:g.22956849del	NCBI36
NG_007884.1:g.22863del , LRG_384:g.22863del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.4170-113del MANE Select	ENSP00000347507.3:n.4170-113del
ENST00000355349.3:c.4170-113del	ENSP00000347507.3:n.4170-113del
NM_000257.3:c.4170-113del	NP_000248.2:n.4170-113del
XM_017021340.1:c.4170-113del	XP_016876829.1:n.4170-113del
NM_000257.4:c.4170-113del MANE Select	NP_000248.2:n.4170-113del