Canonical Allele Identifier: CA2123464773

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415860_23415861delinsAG , CM000676.2:g.23415860_23415861delinsAG GRCh38
NC_000014.8:g.23885069_23885070delinsAG , CM000676.1:g.23885069_23885070delinsAG GRCh37
NC_000014.7:g.22954909_22954910delinsAG NCBI36
NG_007884.1:g.24801_24802delinsCT , LRG_384:g.24801_24802delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4954-29_4954-28delinsCT (MYH7) MANE Select ENSP00000347507.3:n.4954-29_4954-28delinsCT
ENST00000355349.3:c.4954-29_4954-28delinsCT (MYH7) ENSP00000347507.3:n.4954-29_4954-28delinsCT
NM_000257.3:c.4954-29_4954-28delinsCT (MYH7) NP_000248.2:n.4954-29_4954-28delinsCT
NR_126491.1:n.261+31_261+32delinsAG (MHRT)
XM_017021340.1:c.4954-29_4954-28delinsCT (MYH7) XP_016876829.1:n.4954-29_4954-28delinsCT
NM_000257.4:c.4954-29_4954-28delinsCT (MYH7) MANE Select NP_000248.2:n.4954-29_4954-28delinsCT