Canonical Allele Identifier: CA2562627431

Gene: SHC4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48929296A>T , CM000677.2:g.48929296A>T	GRCh38
NC_000015.9:g.49221493A>T , CM000677.1:g.49221493A>T	GRCh37
NC_000015.8:g.47008785A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000332408.9:c.586-4347T>A MANE Select	ENSP00000329668.4:n.586-4347T>A
ENST00000332408.8:c.586-4347T>A	ENSP00000329668.4:n.586-4347T>A
NM_203349.3:c.586-4347T>A	NP_976224.3:n.586-4347T>A
XM_005254375.2:c.37-4347T>A	XP_005254432.1:n.37-4347T>A
XM_011521552.1:c.-3-4347T>A	XP_011519854.1:n.-3-4347T>A
XM_005254375.3:c.37-4347T>A	XP_005254432.1:n.37-4347T>A
NM_203349.4:c.586-4347T>A MANE Select	NP_976224.3:n.586-4347T>A