Canonical Allele Identifier: CA1469632716

Gene: SHROOM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476818_76476821delinsTCAA , CM000666.2:g.76476818_76476821delinsTCAA	GRCh38
NC_000004.11:g.77397971_77397974delinsTCAA , CM000666.1:g.77397971_77397974delinsTCAA	GRCh37
NC_000004.10:g.77616995_77616998delinsTCAA	NCBI36
NG_028077.1:g.46719_46722delinsTCAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000296043.7:c.168+40598_168+40601delinsTCAA MANE Select	ENSP00000296043.6:n.168+40598_168+40601de...
ENST00000296043.6:c.168+40598_168+40601delinsTCAA	ENSP00000296043.6:n.168+40598_168+40601de...
ENST00000466541.1:n.75+40598_75+40601delinsTCAA
ENST00000497440.5:n.109+40598_109+40601delinsTCAA
NM_020859.3:c.168+40598_168+40601delinsTCAA	NP_065910.3:n.168+40598_168+40601delinsTC...
XM_005263162.3:c.168+40598_168+40601delinsTCAA	XP_005263219.1:n.168+40598_168+40601delin...
XM_011532158.1:c.168+40598_168+40601delinsTCAA	XP_011530460.1:n.168+40598_168+40601delin...
XM_011532159.1:c.168+40598_168+40601delinsTCAA	XP_011530461.1:n.168+40598_168+40601delin...
XM_011532158.3:c.168+40598_168+40601delinsTCAA	XP_011530460.1:n.168+40598_168+40601delin...
NM_020859.4:c.168+40598_168+40601delinsTCAA MANE Select	NP_065910.3:n.168+40598_168+40601delinsTC...