Canonical Allele Identifier: CA961069673

Gene: MYH7

Linked Data

• dbSNP Id: rs1892840059
• gnomAD v3: 14-23429538-T-TA
• gnomAD v4: 14-23429538-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23429538_23429539insA , CM000676.2:g.23429538_23429539insA	GRCh38
NC_000014.8:g.23898747_23898748insA , CM000676.1:g.23898747_23898748insA	GRCh37
NC_000014.7:g.22968587_22968588insA	NCBI36
NG_007884.1:g.11123_11124insT , LRG_384:g.11123_11124insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.1139-192_1139-191insT MANE Select	ENSP00000347507.3:n.1139-192_1139-191insT
ENST00000355349.3:c.1139-192_1139-191insT	ENSP00000347507.3:n.1139-192_1139-191insT
NM_000257.3:c.1139-192_1139-191insT	NP_000248.2:n.1139-192_1139-191insT
XR_245686.3:n.1245-192_1245-191insT
XM_017021340.1:c.1139-192_1139-191insT	XP_016876829.1:n.1139-192_1139-191insT
NM_000257.4:c.1139-192_1139-191insT MANE Select	NP_000248.2:n.1139-192_1139-191insT