Canonical Allele Identifier: CA2624236589

Gene: MYH7

Linked Data

• gnomAD v4: 14-23423790-C-CTCCATGTCAAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423797_23423808dup , CM000676.2:g.23423797_23423808dup	GRCh38
NC_000014.8:g.23893006_23893017dup , CM000676.1:g.23893006_23893017dup	GRCh37
NC_000014.7:g.22962846_22962857dup	NCBI36
NG_007884.1:g.16860_16871dup , LRG_384:g.16860_16871dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2923-79_2923-68dup MANE Select	ENSP00000347507.3:n.2923-79_2923-68dup
ENST00000355349.3:c.2923-79_2923-68dup	ENSP00000347507.3:n.2923-79_2923-68dup
NM_000257.3:c.2923-79_2923-68dup	NP_000248.2:n.2923-79_2923-68dup
XR_245686.3:n.3029-79_3029-68dup
XM_017021340.1:c.2923-79_2923-68dup	XP_016876829.1:n.2923-79_2923-68dup
NM_000257.4:c.2923-79_2923-68dup MANE Select	NP_000248.2:n.2923-79_2923-68dup