Canonical Allele Identifier: CA2175727363
Gene: SHC4 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4363T= MANE Select ENSP00000329668.4:n.586-4363T=
ENST00000332408.8:c.586-4363T= ENSP00000329668.4:n.586-4363T=
NM_203349.3:c.586-4363T= NP_976224.3:n.586-4363T=
XM_005254375.2:c.37-4363T= XP_005254432.1:n.37-4363T=
XM_011521552.1:c.-3-4363T= XP_011519854.1:n.-3-4363T=
XM_005254375.3:c.37-4363T= XP_005254432.1:n.37-4363T=
NM_203349.4:c.586-4363T= MANE Select NP_976224.3:n.586-4363T=
Search 100 bp 5'
Search 100 bp 3'