Canonical Allele Identifier: CA2175727365

Gene: SHC4

Linked Data

• dbSNP Id: rs1873649829

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48929313del , CM000677.2:g.48929313del	GRCh38
NC_000015.9:g.49221510del , CM000677.1:g.49221510del	GRCh37
NC_000015.8:g.47008802del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000332408.9:c.586-4364del MANE Select	ENSP00000329668.4:n.586-4364del
ENST00000332408.8:c.586-4364del	ENSP00000329668.4:n.586-4364del
NM_203349.3:c.586-4364del	NP_976224.3:n.586-4364del
XM_005254375.2:c.37-4364del	XP_005254432.1:n.37-4364del
XM_011521552.1:c.-3-4364del	XP_011519854.1:n.-3-4364del
XM_005254375.3:c.37-4364del	XP_005254432.1:n.37-4364del
NM_203349.4:c.586-4364del MANE Select	NP_976224.3:n.586-4364del