Canonical Allele Identifier: CA2624235636
Gene: MYH7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423487_23423488insCGCACACACA , CM000676.2:g.23423487_23423488insCGCACACACA GRCh38
NC_000014.8:g.23892696_23892697insCGCACACACA , CM000676.1:g.23892696_23892697insCGCACACACA GRCh37
NC_000014.7:g.22962536_22962537insCGCACACACA NCBI36
NG_007884.1:g.17182_17183insCGTGTGTGTG , LRG_384:g.17182_17183insCGTGTGTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+67_3099+68insCGTGTGTGTG MANE Select ENSP00000347507.3:n.3099+67_3099+68insCGTGTGTGTG
ENST00000355349.3:c.3099+67_3099+68insCGTGTGTGTG ENSP00000347507.3:n.3099+67_3099+68insCGTGTGTGTG
NM_000257.3:c.3099+67_3099+68insCGTGTGTGTG NP_000248.2:n.3099+67_3099+68insCGTGTGTGTG
XR_245686.3:n.3205+67_3205+68insCGTGTGTGTG
XM_017021340.1:c.3099+67_3099+68insCGTGTGTGTG XP_016876829.1:n.3099+67_3099+68insCGTGTGTGTG
NM_000257.4:c.3099+67_3099+68insCGTGTGTGTG MANE Select NP_000248.2:n.3099+67_3099+68insCGTGTGTGTG