Canonical Allele Identifier: CA2624232544

Gene: MYH7

Linked Data

• gnomAD v4: 14-23420326-C-CTA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420326_23420327insTA , CM000676.2:g.23420326_23420327insTA	GRCh38
NC_000014.8:g.23889535_23889536insTA , CM000676.1:g.23889535_23889536insTA	GRCh37
NC_000014.7:g.22959375_22959376insTA	NCBI36
NG_007884.1:g.20335_20336insTA , LRG_384:g.20335_20336insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3337-93_3337-92insTA MANE Select	ENSP00000347507.3:n.3337-93_3337-92insTA
ENST00000355349.3:c.3337-93_3337-92insTA	ENSP00000347507.3:n.3337-93_3337-92insTA
NM_000257.3:c.3337-93_3337-92insTA	NP_000248.2:n.3337-93_3337-92insTA
XR_245686.3:n.3445-93_3445-92insTA
XM_017021340.1:c.3337-93_3337-92insTA	XP_016876829.1:n.3337-93_3337-92insTA
NM_000257.4:c.3337-93_3337-92insTA MANE Select	NP_000248.2:n.3337-93_3337-92insTA