Canonical Allele Identifier: CA961074495

Gene: MYH7

Linked Data

• dbSNP Id: rs1892564880
• gnomAD v3: 14-23423483-A-ACACACACACACACACC
• gnomAD v4: 14-23423483-A-ACACACACACACACACC

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423487_23423488insCACACACACACCCACA , CM000676.2:g.23423487_23423488insCACACACACACCCACA	GRCh38
NC_000014.8:g.23892696_23892697insCACACACACACCCACA , CM000676.1:g.23892696_23892697insCACACACACACCCACA	GRCh37
NC_000014.7:g.22962536_22962537insCACACACACACCCACA	NCBI36
NG_007884.1:g.17178_17179insGGTGTGTGTGTGTGTG , LRG_384:g.17178_17179insGGTGTGTGTGTGTGTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3099+63_3099+64insGGTGTGTGTGTGTGTG MANE Select	ENSP00000347507.3:n.3099+63_3099+64insGGTGTGTGTGTGTGTG
ENST00000355349.3:c.3099+63_3099+64insGGTGTGTGTGTGTGTG	ENSP00000347507.3:n.3099+63_3099+64insGGTGTGTGTGTGTGTG
NM_000257.3:c.3099+63_3099+64insGGTGTGTGTGTGTGTG	NP_000248.2:n.3099+63_3099+64insGGTGTGTGTGTGTGTG
XR_245686.3:n.3205+63_3205+64insGGTGTGTGTGTGTGTG
XM_017021340.1:c.3099+63_3099+64insGGTGTGTGTGTGTGTG	XP_016876829.1:n.3099+63_3099+64insGGTGTGTGTGTGTGTG
NM_000257.4:c.3099+63_3099+64insGGTGTGTGTGTGTGTG MANE Select	NP_000248.2:n.3099+63_3099+64insGGTGTGTGTGTGTGTG