Canonical Allele Identifier: CA485766590

Gene: MYH7

Linked Data

• MyVariant Identifiers: chr14:g.23892881G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23423672G>A , CM000676.2:g.23423672G>A	GRCh38
NC_000014.8:g.23892881G>A , CM000676.1:g.23892881G>A	GRCh37
NC_000014.7:g.22962721G>A	NCBI36
NG_007884.1:g.16990C>T , LRG_384:g.16990C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.2974C>T MANE Select	ENSP00000347507.3:p.Leu992=
ENST00000355349.3:c.2974C>T	ENSP00000347507.3:p.Leu992=
NM_000257.3:c.2974C>T	NP_000248.2:p.Leu992=
XR_245686.3:n.3080C>T
XM_017021340.1:c.2974C>T	XP_016876829.1:p.Leu992=
NM_000257.4:c.2974C>T MANE Select	NP_000248.2:p.Leu992=