Canonical Allele Identifier: CA1469632395

Gene: SHROOM3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476534_76476535delinsAT , CM000666.2:g.76476534_76476535delinsAT	GRCh38
NC_000004.11:g.77397687_77397688delinsAT , CM000666.1:g.77397687_77397688delinsAT	GRCh37
NC_000004.10:g.77616711_77616712delinsAT	NCBI36
NG_028077.1:g.46435_46436delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296043.7:c.168+40314_168+40315delinsAT MANE Select	ENSP00000296043.6:n.168+40314_168+40315delinsAT
ENST00000296043.6:c.168+40314_168+40315delinsAT	ENSP00000296043.6:n.168+40314_168+40315delinsAT
ENST00000466541.1:n.75+40314_75+40315delinsAT
ENST00000497440.5:n.109+40314_109+40315delinsAT
NM_020859.3:c.168+40314_168+40315delinsAT	NP_065910.3:n.168+40314_168+40315delinsAT
XM_005263162.3:c.168+40314_168+40315delinsAT	XP_005263219.1:n.168+40314_168+40315delinsAT
XM_011532158.1:c.168+40314_168+40315delinsAT	XP_011530460.1:n.168+40314_168+40315delinsAT
XM_011532159.1:c.168+40314_168+40315delinsAT	XP_011530461.1:n.168+40314_168+40315delinsAT
XM_011532158.3:c.168+40314_168+40315delinsAT	XP_011530460.1:n.168+40314_168+40315delinsAT
NM_020859.4:c.168+40314_168+40315delinsAT MANE Select	NP_065910.3:n.168+40314_168+40315delinsAT