Canonical Allele Identifier: CA612937358

Gene: MYH7

Linked Data

• gnomAD v2: 14-23892672-A-ACACACACACACACACACACACACACACACACC
• gnomAD v3: 14-23423463-A-ACACACACACACACACACACACACACACACACC
• gnomAD v4: 14-23423463-A-ACACACACACACACACACACACACACACACACC
• MyVariant Identifiers: chr14:g.23892672_23892673insCACACACACACACACACACACACACACACACC (hg19) ; chr14:g.23423463_23423464insCACACACACACACACACACACACACACACACC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423487_23423488insCACACACCCACACACACACACACACACACACA , CM000676.2:g.23423487_23423488insCACACACCCACACACACACACACACACACACA	GRCh38
NC_000014.8:g.23892696_23892697insCACACACCCACACACACACACACACACACACA , CM000676.1:g.23892696_23892697insCACACACCCACACACACACACACACACACACA	GRCh37
NC_000014.7:g.22962536_22962537insCACACACCCACACACACACACACACACACACA	NCBI36
NG_007884.1:g.17198_17199insGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG , LRG_384:g.17198_17199insGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+83_3099+84insGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG MANE Select	ENSP00000347507.3:n.3099+83_3099+84insGGTGTGTGTGTGTGTGTGTGTGT...
ENST00000355349.3:c.3099+83_3099+84insGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	ENSP00000347507.3:n.3099+83_3099+84insGGTGTGTGTGTGTGTGTGTGTGT...
NM_000257.3:c.3099+83_3099+84insGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	NP_000248.2:n.3099+83_3099+84insGGTGTGTGTGTGTGTGTGTGTGTGTGTGT...
XR_245686.3:n.3205+83_3205+84insGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG
XM_017021340.1:c.3099+83_3099+84insGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG	XP_016876829.1:n.3099+83_3099+84insGGTGTGTGTGTGTGTGTGTGTGTGTG...
NM_000257.4:c.3099+83_3099+84insGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTG MANE Select	NP_000248.2:n.3099+83_3099+84insGGTGTGTGTGTGTGTGTGTGTGTGTGTGT...