Canonical Allele Identifier: CA2624235626

Gene: MYH7

Linked Data

• gnomAD v4: 14-23423479-A-ACACACACACACACG

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423487_23423488insCACACGCACACACA , CM000676.2:g.23423487_23423488insCACACGCACACACA	GRCh38
NC_000014.8:g.23892696_23892697insCACACGCACACACA , CM000676.1:g.23892696_23892697insCACACGCACACACA	GRCh37
NC_000014.7:g.22962536_22962537insCACACGCACACACA	NCBI36
NG_007884.1:g.17182_17183insCGTGTGTGTGTGTG , LRG_384:g.17182_17183insCGTGTGTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+67_3099+68insCGTGTGTGTGTGTG MANE Select	ENSP00000347507.3:n.3099+67_3099+68insCGTGTGTGTGTGTG
ENST00000355349.3:c.3099+67_3099+68insCGTGTGTGTGTGTG	ENSP00000347507.3:n.3099+67_3099+68insCGTGTGTGTGTGTG
NM_000257.3:c.3099+67_3099+68insCGTGTGTGTGTGTG	NP_000248.2:n.3099+67_3099+68insCGTGTGTGTGTGTG
XR_245686.3:n.3205+67_3205+68insCGTGTGTGTGTGTG
XM_017021340.1:c.3099+67_3099+68insCGTGTGTGTGTGTG	XP_016876829.1:n.3099+67_3099+68insCGTGTGTGTGTGTG
NM_000257.4:c.3099+67_3099+68insCGTGTGTGTGTGTG MANE Select	NP_000248.2:n.3099+67_3099+68insCGTGTGTGTGTGTG