Canonical Allele Identifier: CA2624236592

Gene: MYH7

Linked Data

• gnomAD v4: 14-23423790-CTCCATGTCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423791_23423799del , CM000676.2:g.23423791_23423799del	GRCh38
NC_000014.8:g.23893000_23893008del , CM000676.1:g.23893000_23893008del	GRCh37
NC_000014.7:g.22962840_22962848del	NCBI36
NG_007884.1:g.16863_16871del , LRG_384:g.16863_16871del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2923-76_2923-68del MANE Select	ENSP00000347507.3:n.2923-76_2923-68del
ENST00000355349.3:c.2923-76_2923-68del	ENSP00000347507.3:n.2923-76_2923-68del
NM_000257.3:c.2923-76_2923-68del	NP_000248.2:n.2923-76_2923-68del
XR_245686.3:n.3029-76_3029-68del
XM_017021340.1:c.2923-76_2923-68del	XP_016876829.1:n.2923-76_2923-68del
NM_000257.4:c.2923-76_2923-68del MANE Select	NP_000248.2:n.2923-76_2923-68del