Canonical Allele Identifier: CA2466528037

Gene: ARHGAP4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153924366C= , CM000685.2:g.153924366C=	GRCh38
NC_000023.10:g.153189819C= , CM000685.1:g.153189819C=	GRCh37
NC_000023.9:g.152843013C=	NCBI36
NG_013220.1:g.6896G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350060.10:c.67+1770G= MANE Select	ENSP00000203786.8:n.67+1770G=
ENST00000350060.9:c.67+1770G=	ENSP00000203786.7:n.67+1770G=
ENST00000370016.5:c.67+1770G=	ENSP00000359033.1:n.67+1770G=
ENST00000370028.7:c.67+1770G=	ENSP00000359045.3:n.67+1770G=
ENST00000393721.5:c.67+1770G=	ENSP00000377322.1:n.67+1770G=
ENST00000404127.6:c.67+1770G=	ENSP00000385042.2:n.67+1770G=
ENST00000420383.5:c.67+1770G=	ENSP00000397533.1:n.67+1770G=
ENST00000422091.1:c.-3+2450G=	ENSP00000413782.1:n.-3+2450G=
ENST00000442262.5:c.-2-2557G=	ENSP00000398259.1:n.-2-2557G=
ENST00000461052.5:c.-3+2224G=	ENSP00000473840.1:n.-3+2224G=
ENST00000470209.5:n.109+1770G=
ENST00000470979.1:n.29-2557G=
ENST00000494302.5:n.109+1770G=
ENST00000494813.5:n.482-2557G=
NM_001164741.1:c.67+1770G=	NP_001158213.1:n.67+1770G=
NM_001666.4:c.67+1770G=	NP_001657.3:n.67+1770G=
NM_001164741.2:c.67+1770G=	NP_001158213.1:n.67+1770G=
NM_001666.5:c.67+1770G= MANE Select	NP_001657.3:n.67+1770G=