Canonical Allele Identifier: CA2175727367
Gene: SHC4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929314G= , CM000677.2:g.48929314G= GRCh38
NC_000015.9:g.49221511G= , CM000677.1:g.49221511G= GRCh37
NC_000015.8:g.47008803G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4365C= MANE Select ENSP00000329668.4:n.586-4365C=
ENST00000332408.8:c.586-4365C= ENSP00000329668.4:n.586-4365C=
NM_203349.3:c.586-4365C= NP_976224.3:n.586-4365C=
XM_005254375.2:c.37-4365C= XP_005254432.1:n.37-4365C=
XM_011521552.1:c.-3-4365C= XP_011519854.1:n.-3-4365C=
XM_005254375.3:c.37-4365C= XP_005254432.1:n.37-4365C=
NM_203349.4:c.586-4365C= MANE Select NP_976224.3:n.586-4365C=