Canonical Allele Identifier: CA2624232596

Gene: MYH7

Linked Data

• gnomAD v4: 14-23420373-G-GGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420374_23420375insCTG , CM000676.2:g.23420374_23420375insCTG	GRCh38
NC_000014.8:g.23889583_23889584insCTG , CM000676.1:g.23889583_23889584insCTG	GRCh37
NC_000014.7:g.22959423_22959424insCTG	NCBI36
NG_007884.1:g.20288_20289insAGC , LRG_384:g.20288_20289insAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3337-140_3337-139insAGC MANE Select	ENSP00000347507.3:n.3337-140_3337-139insAGC
ENST00000355349.3:c.3337-140_3337-139insAGC	ENSP00000347507.3:n.3337-140_3337-139insAGC
NM_000257.3:c.3337-140_3337-139insAGC	NP_000248.2:n.3337-140_3337-139insAGC
XR_245686.3:n.3445-140_3445-139insAGC
XM_017021340.1:c.3337-140_3337-139insAGC	XP_016876829.1:n.3337-140_3337-139insAGC
NM_000257.4:c.3337-140_3337-139insAGC MANE Select	NP_000248.2:n.3337-140_3337-139insAGC