Canonical Allele Identifier: CA1469632890

Gene: SHROOM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476990_76476992delinsCAG , CM000666.2:g.76476990_76476992delinsCAG	GRCh38
NC_000004.11:g.77398143_77398145delinsCAG , CM000666.1:g.77398143_77398145delinsCAG	GRCh37
NC_000004.10:g.77617167_77617169delinsCAG	NCBI36
NG_028077.1:g.46891_46893delinsCAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000296043.7:c.168+40770_168+40772delinsCAG MANE Select	ENSP00000296043.6:n.168+40770_168+40772delinsCAG
ENST00000296043.6:c.168+40770_168+40772delinsCAG	ENSP00000296043.6:n.168+40770_168+40772delinsCAG
ENST00000466541.1:n.75+40770_75+40772delinsCAG
ENST00000497440.5:n.109+40770_109+40772delinsCAG
NM_020859.3:c.168+40770_168+40772delinsCAG	NP_065910.3:n.168+40770_168+40772delinsCAG
XM_005263162.3:c.168+40770_168+40772delinsCAG	XP_005263219.1:n.168+40770_168+40772delinsCAG
XM_011532158.1:c.168+40770_168+40772delinsCAG	XP_011530460.1:n.168+40770_168+40772delinsCAG
XM_011532159.1:c.168+40770_168+40772delinsCAG	XP_011530461.1:n.168+40770_168+40772delinsCAG
XM_011532158.3:c.168+40770_168+40772delinsCAG	XP_011530460.1:n.168+40770_168+40772delinsCAG
NM_020859.4:c.168+40770_168+40772delinsCAG MANE Select	NP_065910.3:n.168+40770_168+40772delinsCAG