Canonical Allele Identifier: CA2175727381
Gene: SHC4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929347C= , CM000677.2:g.48929347C= GRCh38
NC_000015.9:g.49221544C= , CM000677.1:g.49221544C= GRCh37
NC_000015.8:g.47008836C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4398G= MANE Select ENSP00000329668.4:n.586-4398G=
ENST00000332408.8:c.586-4398G= ENSP00000329668.4:n.586-4398G=
NM_203349.3:c.586-4398G= NP_976224.3:n.586-4398G=
XM_005254375.2:c.37-4398G= XP_005254432.1:n.37-4398G=
XM_011521552.1:c.-3-4398G= XP_011519854.1:n.-3-4398G=
XM_005254375.3:c.37-4398G= XP_005254432.1:n.37-4398G=
NM_203349.4:c.586-4398G= MANE Select NP_976224.3:n.586-4398G=
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