Canonical Allele Identifier: CA100204492

Gene: SHROOM3

Linked Data

• dbSNP Id: rs386676255

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476676_76476677delinsTC , CM000666.2:g.76476676_76476677delinsTC	GRCh38
NC_000004.11:g.77397829_77397830delinsTC , CM000666.1:g.77397829_77397830delinsTC	GRCh37
NC_000004.10:g.77616853_77616854delinsTC	NCBI36
NG_028077.1:g.46577_46578delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000296043.7:c.168+40456_168+40457delinsTC MANE Select	ENSP00000296043.6:n.168+40456_168+40457delinsTC
ENST00000296043.6:c.168+40456_168+40457delinsTC	ENSP00000296043.6:n.168+40456_168+40457delinsTC
ENST00000466541.1:n.75+40456_75+40457delinsTC
ENST00000497440.5:n.109+40456_109+40457delinsTC
NM_020859.3:c.168+40456_168+40457delinsTC	NP_065910.3:n.168+40456_168+40457delinsTC
XM_005263162.3:c.168+40456_168+40457delinsTC	XP_005263219.1:n.168+40456_168+40457delinsTC
XM_011532158.1:c.168+40456_168+40457delinsTC	XP_011530460.1:n.168+40456_168+40457delinsTC
XM_011532159.1:c.168+40456_168+40457delinsTC	XP_011530461.1:n.168+40456_168+40457delinsTC
XM_011532158.3:c.168+40456_168+40457delinsTC	XP_011530460.1:n.168+40456_168+40457delinsTC
NM_020859.4:c.168+40456_168+40457delinsTC MANE Select	NP_065910.3:n.168+40456_168+40457delinsTC