Canonical Allele Identifier: CA2808461704
Gene: MYH8 HGNC NCBI
MYHAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.10404250_10404251insTTTTTTTTT , CM000679.2:g.10404250_10404251insTTTTTTTTT GRCh38
NC_000017.10:g.10307567_10307568insTTTTTTTTT , CM000679.1:g.10307567_10307568insTTTTTTTTT GRCh37
NC_000017.9:g.10248292_10248293insTTTTTTTTT NCBI36
NG_013015.1:g.22700_22701insAAAAAAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000403437.2:c.2688+79_2688+80insAAAAAAAAA (MYH8) MANE Select ENSP00000384330.2:n.2688+79_2688+80insAAAAAAAAA
NM_002472.2:c.2688+79_2688+80insAAAAAAAAA (MYH8) NP_002463.2:n.2688+79_2688+80insAAAAAAAAA
NR_125367.1:n.77-1898_77-1897insTTTTTTTTT (MYHAS)
XM_011523873.1:c.2784+79_2784+80insAAAAAAAAA (MYH8) XP_011522175.1:n.2784+79_2784+80insAAAAAAAAA
XM_011523874.1:c.2784+79_2784+80insAAAAAAAAA (MYH8) XP_011522176.1:n.2784+79_2784+80insAAAAAAAAA
NM_002472.3:c.2688+79_2688+80insAAAAAAAAA (MYH8) MANE Select NP_002463.2:n.2688+79_2688+80insAAAAAAAAA
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