Canonical Allele Identifier: CA2123464990

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415991T= , CM000676.2:g.23415991T= GRCh38
NC_000014.8:g.23885200T= , CM000676.1:g.23885200T= GRCh37
NC_000014.7:g.22955040T= NCBI36
NG_007884.1:g.24671A= , LRG_384:g.24671A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4953+13A= (MYH7) MANE Select ENSP00000347507.3:n.4953+13A=
ENST00000355349.3:c.4953+13A= (MYH7) ENSP00000347507.3:n.4953+13A=
NM_000257.3:c.4953+13A= (MYH7) NP_000248.2:n.4953+13A=
NR_126491.1:n.262-10T= (MHRT)
XM_017021340.1:c.4953+13A= (MYH7) XP_016876829.1:n.4953+13A=
NM_000257.4:c.4953+13A= (MYH7) MANE Select NP_000248.2:n.4953+13A=