Canonical Allele Identifier: CA1469632626

Gene: SHROOM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476756_76476758delinsCTT , CM000666.2:g.76476756_76476758delinsCTT	GRCh38
NC_000004.11:g.77397909_77397911delinsCTT , CM000666.1:g.77397909_77397911delinsCTT	GRCh37
NC_000004.10:g.77616933_77616935delinsCTT	NCBI36
NG_028077.1:g.46657_46659delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000296043.7:c.168+40536_168+40538delinsCTT MANE Select	ENSP00000296043.6:n.168+40536_168+40538delinsCTT
ENST00000296043.6:c.168+40536_168+40538delinsCTT	ENSP00000296043.6:n.168+40536_168+40538delinsCTT
ENST00000466541.1:n.75+40536_75+40538delinsCTT
ENST00000497440.5:n.109+40536_109+40538delinsCTT
NM_020859.3:c.168+40536_168+40538delinsCTT	NP_065910.3:n.168+40536_168+40538delinsCTT
XM_005263162.3:c.168+40536_168+40538delinsCTT	XP_005263219.1:n.168+40536_168+40538delinsCTT
XM_011532158.1:c.168+40536_168+40538delinsCTT	XP_011530460.1:n.168+40536_168+40538delinsCTT
XM_011532159.1:c.168+40536_168+40538delinsCTT	XP_011530461.1:n.168+40536_168+40538delinsCTT
XM_011532158.3:c.168+40536_168+40538delinsCTT	XP_011530460.1:n.168+40536_168+40538delinsCTT
NM_020859.4:c.168+40536_168+40538delinsCTT MANE Select	NP_065910.3:n.168+40536_168+40538delinsCTT