Canonical Allele Identifier: CA2624250299

Gene: MYH7

Linked Data

• gnomAD v4: 14-23430759-GGGCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23430768_23430772del , CM000676.2:g.23430768_23430772del	GRCh38
NC_000014.8:g.23899977_23899981del , CM000676.1:g.23899977_23899981del	GRCh37
NC_000014.7:g.22969817_22969821del	NCBI36
NG_007884.1:g.9898_9902del , LRG_384:g.9898_9902del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.896-101_896-97del MANE Select	ENSP00000347507.3:n.896-101_896-97del
ENST00000355349.3:c.896-101_896-97del	ENSP00000347507.3:n.896-101_896-97del
NM_000257.3:c.896-101_896-97del	NP_000248.2:n.896-101_896-97del
XR_245686.3:n.1002-101_1002-97del
XM_017021340.1:c.896-101_896-97del	XP_016876829.1:n.896-101_896-97del
NM_000257.4:c.896-101_896-97del MANE Select	NP_000248.2:n.896-101_896-97del