Canonical Allele Identifier: CA2175727364
Gene: SHC4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929312_48929313delinsAC , CM000677.2:g.48929312_48929313delinsAC GRCh38
NC_000015.9:g.49221509_49221510delinsAC , CM000677.1:g.49221509_49221510delinsAC GRCh37
NC_000015.8:g.47008801_47008802delinsAC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4364_586-4363delinsGT MANE Select ENSP00000329668.4:n.586-4364_586-4363deli...
ENST00000332408.8:c.586-4364_586-4363delinsGT ENSP00000329668.4:n.586-4364_586-4363deli...
NM_203349.3:c.586-4364_586-4363delinsGT NP_976224.3:n.586-4364_586-4363delinsGT
XM_005254375.2:c.37-4364_37-4363delinsGT XP_005254432.1:n.37-4364_37-4363delinsGT
XM_011521552.1:c.-3-4364_-3-4363delinsGT XP_011519854.1:n.-3-4364_-3-4363delinsGT
XM_005254375.3:c.37-4364_37-4363delinsGT XP_005254432.1:n.37-4364_37-4363delinsGT
NM_203349.4:c.586-4364_586-4363delinsGT MANE Select NP_976224.3:n.586-4364_586-4363delinsGT
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