Canonical Allele Identifier: CA2123448066

Gene: MYH7

Linked Data

• dbSNP Id: rs1892439433

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23420676_23420677insT , CM000676.2:g.23420676_23420677insT	GRCh38
NC_000014.8:g.23889885_23889886insT , CM000676.1:g.23889885_23889886insT	GRCh37
NC_000014.7:g.22959725_22959726insT	NCBI36
NG_007884.1:g.19985_19986insA , LRG_384:g.19985_19986insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.3336+281_3336+282insA MANE Select	ENSP00000347507.3:n.3336+281_3336+282insA
ENST00000355349.3:c.3336+281_3336+282insA	ENSP00000347507.3:n.3336+281_3336+282insA
NM_000257.3:c.3336+281_3336+282insA	NP_000248.2:n.3336+281_3336+282insA
XR_245686.3:n.3444+281_3444+282insA
XM_017021340.1:c.3336+281_3336+282insA	XP_016876829.1:n.3336+281_3336+282insA
NM_000257.4:c.3336+281_3336+282insA MANE Select	NP_000248.2:n.3336+281_3336+282insA