Canonical Allele Identifier: CA2123466007

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23416275_23416276delinsGC , CM000676.2:g.23416275_23416276delinsGC GRCh38
NC_000014.8:g.23885484_23885485delinsGC , CM000676.1:g.23885484_23885485delinsGC GRCh37
NC_000014.7:g.22955324_22955325delinsGC NCBI36
NG_007884.1:g.24386_24387delinsGC , LRG_384:g.24386_24387delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4681_4682delinsGC (MYH7) MANE Select ENSP00000347507.3:p.Ala1561=
ENST00000355349.3:c.4681_4682delinsGC (MYH7) ENSP00000347507.3:p.Ala1561=
NM_000257.3:c.4681_4682delinsGC (MYH7) NP_000248.2:p.Ala1561=
NR_126491.1:n.536_537delinsGC (MHRT)
XM_017021340.1:c.4681_4682delinsGC (MYH7) XP_016876829.1:p.Ala1561=
NM_000257.4:c.4681_4682delinsGC (MYH7) MANE Select NP_000248.2:p.Ala1561=