Canonical Allele Identifier: CA257810276

Linked Data

dbSNP Id: rs34479915

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.23415963_23415964insA , CM000676.2:g.23415963_23415964insA GRCh38
NC_000014.8:g.23885172_23885173insA , CM000676.1:g.23885172_23885173insA GRCh37
NC_000014.7:g.22955012_22955013insA NCBI36
NG_007884.1:g.24698_24699insT , LRG_384:g.24698_24699insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000355349.4:c.4953+40_4953+41insT (MYH7) MANE Select ENSP00000347507.3:n.4953+40_4953+41insT
ENST00000355349.3:c.4953+40_4953+41insT (MYH7) ENSP00000347507.3:n.4953+40_4953+41insT
NM_000257.3:c.4953+40_4953+41insT (MYH7) NP_000248.2:n.4953+40_4953+41insT
NR_126491.1:n.262-38_262-37insA (MHRT)
XM_017021340.1:c.4953+40_4953+41insT (MYH7) XP_016876829.1:n.4953+40_4953+41insT
NM_000257.4:c.4953+40_4953+41insT (MYH7) MANE Select NP_000248.2:n.4953+40_4953+41insT