Canonical Allele Identifier: CA2600527073

Gene: SHROOM3

Linked Data

• gnomAD v3: 4-76476970-AATTT-A
• gnomAD v4: 4-76476970-AATTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.76476979_76476982del , CM000666.2:g.76476979_76476982del	GRCh38
NC_000004.11:g.77398132_77398135del , CM000666.1:g.77398132_77398135del	GRCh37
NC_000004.10:g.77617156_77617159del	NCBI36
NG_028077.1:g.46880_46883del

Transcript Alleles

HGVS	Amino-acid change
ENST00000296043.7:c.168+40759_168+40762del MANE Select	ENSP00000296043.6:n.168+40759_168+40762del
ENST00000296043.6:c.168+40759_168+40762del	ENSP00000296043.6:n.168+40759_168+40762del
ENST00000466541.1:n.75+40759_75+40762del
ENST00000497440.5:n.109+40759_109+40762del
NM_020859.3:c.168+40759_168+40762del	NP_065910.3:n.168+40759_168+40762del
XM_005263162.3:c.168+40759_168+40762del	XP_005263219.1:n.168+40759_168+40762del
XM_011532158.1:c.168+40759_168+40762del	XP_011530460.1:n.168+40759_168+40762del
XM_011532159.1:c.168+40759_168+40762del	XP_011530461.1:n.168+40759_168+40762del
XM_011532158.3:c.168+40759_168+40762del	XP_011530460.1:n.168+40759_168+40762del
NM_020859.4:c.168+40759_168+40762del MANE Select	NP_065910.3:n.168+40759_168+40762del