Canonical Allele Identifier: CA2838498500

Gene: ARHGEF40

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.21078110del , CM000676.2:g.21078110del	GRCh38
NC_000014.8:g.21546269del , CM000676.1:g.21546269del	GRCh37
NC_000014.7:g.20616109del	NCBI36
NG_034001.1:g.12851del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000298694.9:c.2035-67del MANE Select	ENSP00000298694.4:n.2035-67del
ENST00000298694.8:c.2035-67del	ENSP00000298694.4:n.2035-67del
ENST00000553709.5:c.*199-67del	ENSP00000452283.1:n.*199-67del
ENST00000555232.5:n.462-67del
ENST00000556399.5:c.*359-67del	ENSP00000451655.1:n.*359-67del
NM_001278529.1:c.-108-67del	NP_001265458.1:n.-108-67del
NM_001278530.1:c.-108-67del	NP_001265459.1:n.-108-67del
NM_018071.4:c.2035-67del	NP_060541.3:n.2035-67del
XM_005267844.1:c.2035-67del	XP_005267901.1:n.2035-67del
XM_011536937.1:c.2035-67del	XP_011535239.1:n.2035-67del
XM_011536938.1:c.2035-67del	XP_011535240.1:n.2035-67del
XM_005267844.3:c.2035-67del	XP_005267901.1:n.2035-67del
XM_011536937.3:c.2035-67del	XP_011535239.1:n.2035-67del
XM_011536938.3:c.2035-67del	XP_011535240.1:n.2035-67del
XM_017021434.2:c.1459-67del	XP_016876923.1:n.1459-67del
XM_017021435.2:c.-108-67del	XP_016876924.1:n.-108-67del
XM_017021436.2:c.-108-67del	XP_016876925.1:n.-108-67del
XM_017021437.2:c.-108-67del	XP_016876926.1:n.-108-67del
NM_018071.5:c.2035-67del MANE Select	NP_060541.3:n.2035-67del
NM_001278529.2:c.-108-67del	NP_001265458.1:n.-108-67del
NM_001278530.2:c.-108-67del	NP_001265459.1:n.-108-67del