Canonical Allele Identifier: CA961074421
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1892560389

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23423436_23423437insC , CM000676.2:g.23423436_23423437insC GRCh38
NC_000014.8:g.23892645_23892646insC , CM000676.1:g.23892645_23892646insC GRCh37
NC_000014.7:g.22962485_22962486insC NCBI36
NG_007884.1:g.17225_17226insG , LRG_384:g.17225_17226insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.3099+110_3099+111insG MANE Select ENSP00000347507.3:n.3099+110_3099+111insG
ENST00000355349.3:c.3099+110_3099+111insG ENSP00000347507.3:n.3099+110_3099+111insG
NM_000257.3:c.3099+110_3099+111insG NP_000248.2:n.3099+110_3099+111insG
XR_245686.3:n.3205+110_3205+111insG
XM_017021340.1:c.3099+110_3099+111insG XP_016876829.1:n.3099+110_3099+111insG
NM_000257.4:c.3099+110_3099+111insG MANE Select NP_000248.2:n.3099+110_3099+111insG