Canonical Allele Identifier: CA2123469187

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23417493C= , CM000676.2:g.23417493C= GRCh38
NC_000014.8:g.23886702C= , CM000676.1:g.23886702C= GRCh37
NC_000014.7:g.22956542C= NCBI36
NG_007884.1:g.23169G= , LRG_384:g.23169G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4353+10G= (MYH7) MANE Select ENSP00000347507.3:n.4353+10G=
ENST00000355349.3:c.4353+10G= (MYH7) ENSP00000347507.3:n.4353+10G=
NM_000257.3:c.4353+10G= (MYH7) NP_000248.2:n.4353+10G=
NR_126491.1:n.814-40C= (MHRT)
XM_017021340.1:c.4353+10G= (MYH7) XP_016876829.1:n.4353+10G=
NM_000257.4:c.4353+10G= (MYH7) MANE Select NP_000248.2:n.4353+10G=