Canonical Allele Identifier: CA269565223
Gene: SHC4 HGNC NCBI

Linked Data

dbSNP Id: rs549983037

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.48929345del , CM000677.2:g.48929345del GRCh38
NC_000015.9:g.49221542del , CM000677.1:g.49221542del GRCh37
NC_000015.8:g.47008834del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000332408.9:c.586-4396del MANE Select ENSP00000329668.4:n.586-4396del
ENST00000332408.8:c.586-4396del ENSP00000329668.4:n.586-4396del
NM_203349.3:c.586-4396del NP_976224.3:n.586-4396del
XM_005254375.2:c.37-4396del XP_005254432.1:n.37-4396del
XM_011521552.1:c.-3-4396del XP_011519854.1:n.-3-4396del
XM_005254375.3:c.37-4396del XP_005254432.1:n.37-4396del
NM_203349.4:c.586-4396del MANE Select NP_976224.3:n.586-4396del