Canonical Allele Identifier: CA2175727359
Gene: SHC4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929301_48929304delinsACTT , CM000677.2:g.48929301_48929304delinsACTT GRCh38
NC_000015.9:g.49221498_49221501delinsACTT , CM000677.1:g.49221498_49221501delinsACTT GRCh37
NC_000015.8:g.47008790_47008793delinsACTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4355_586-4352delinsAAGT MANE Select ENSP00000329668.4:n.586-4355_586-4352deli...
ENST00000332408.8:c.586-4355_586-4352delinsAAGT ENSP00000329668.4:n.586-4355_586-4352deli...
NM_203349.3:c.586-4355_586-4352delinsAAGT NP_976224.3:n.586-4355_586-4352delinsAAGT...
XM_005254375.2:c.37-4355_37-4352delinsAAGT XP_005254432.1:n.37-4355_37-4352delinsAAG...
XM_011521552.1:c.-3-4355_-3-4352delinsAAGT XP_011519854.1:n.-3-4355_-3-4352delinsAAG...
XM_005254375.3:c.37-4355_37-4352delinsAAGT XP_005254432.1:n.37-4355_37-4352delinsAAG...
NM_203349.4:c.586-4355_586-4352delinsAAGT MANE Select NP_976224.3:n.586-4355_586-4352delinsAAGT...
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