Canonical Allele Identifier: CA2123469133
Gene: MYH7 HGNC NCBI
MHRT HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417484G= , CM000676.2:g.23417484G= GRCh38
NC_000014.8:g.23886693G= , CM000676.1:g.23886693G= GRCh37
NC_000014.7:g.22956533G= NCBI36
NG_007884.1:g.23178C= , LRG_384:g.23178C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4353+19C= (MYH7) MANE Select ENSP00000347507.3:n.4353+19C=
ENST00000355349.3:c.4353+19C= (MYH7) ENSP00000347507.3:n.4353+19C=
NM_000257.3:c.4353+19C= (MYH7) NP_000248.2:n.4353+19C=
NR_126491.1:n.814-49G= (MHRT)
XM_017021340.1:c.4353+19C= (MYH7) XP_016876829.1:n.4353+19C=
NM_000257.4:c.4353+19C= (MYH7) MANE Select NP_000248.2:n.4353+19C=
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