Canonical Allele Identifier: CA2123450986
Gene: MYH7 HGNC NCBI

Linked Data

dbSNP Id: rs1892921525

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23431205_23431206insCGTCA , CM000676.2:g.23431205_23431206insCGTCA GRCh38
NC_000014.8:g.23900414_23900415insCGTCA , CM000676.1:g.23900414_23900415insCGTCA GRCh37
NC_000014.7:g.22970254_22970255insCGTCA NCBI36
NG_007884.1:g.9456_9457insTGACG , LRG_384:g.9456_9457insTGACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.797-207_797-206insTGACG MANE Select ENSP00000347507.3:n.797-207_797-206insTGACG
ENST00000355349.3:c.797-207_797-206insTGACG ENSP00000347507.3:n.797-207_797-206insTGACG
NM_000257.3:c.797-207_797-206insTGACG NP_000248.2:n.797-207_797-206insTGACG
XR_245686.3:n.903-207_903-206insTGACG
XM_017021340.1:c.797-207_797-206insTGACG XP_016876829.1:n.797-207_797-206insTGACG
NM_000257.4:c.797-207_797-206insTGACG MANE Select NP_000248.2:n.797-207_797-206insTGACG