Canonical Allele Identifier: CA2175727376
Gene: SHC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929343G= , CM000677.2:g.48929343G= GRCh38
NC_000015.9:g.49221540G= , CM000677.1:g.49221540G= GRCh37
NC_000015.8:g.47008832G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4394C= MANE Select ENSP00000329668.4:n.586-4394C=
ENST00000332408.8:c.586-4394C= ENSP00000329668.4:n.586-4394C=
NM_203349.3:c.586-4394C= NP_976224.3:n.586-4394C=
XM_005254375.2:c.37-4394C= XP_005254432.1:n.37-4394C=
XM_011521552.1:c.-3-4394C= XP_011519854.1:n.-3-4394C=
XM_005254375.3:c.37-4394C= XP_005254432.1:n.37-4394C=
NM_203349.4:c.586-4394C= MANE Select NP_976224.3:n.586-4394C=