Canonical Allele Identifier: CA2175727377
Gene: SHC4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929344_48929345delinsGC , CM000677.2:g.48929344_48929345delinsGC GRCh38
NC_000015.9:g.49221541_49221542delinsGC , CM000677.1:g.49221541_49221542delinsGC GRCh37
NC_000015.8:g.47008833_47008834delinsGC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4396_586-4395delinsGC MANE Select ENSP00000329668.4:n.586-4396_586-4395deli...
ENST00000332408.8:c.586-4396_586-4395delinsGC ENSP00000329668.4:n.586-4396_586-4395deli...
NM_203349.3:c.586-4396_586-4395delinsGC NP_976224.3:n.586-4396_586-4395delinsGC
XM_005254375.2:c.37-4396_37-4395delinsGC XP_005254432.1:n.37-4396_37-4395delinsGC
XM_011521552.1:c.-3-4396_-3-4395delinsGC XP_011519854.1:n.-3-4396_-3-4395delinsGC
XM_005254375.3:c.37-4396_37-4395delinsGC XP_005254432.1:n.37-4396_37-4395delinsGC
NM_203349.4:c.586-4396_586-4395delinsGC MANE Select NP_976224.3:n.586-4396_586-4395delinsGC
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