Canonical Allele Identifier: CA2838524942

Gene: ARHGAP6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.11261098A>G , CM000685.2:g.11261098A>G	GRCh38
NC_000023.10:g.11279218A>G , CM000685.1:g.11279218A>G	GRCh37
NC_000023.9:g.11189139A>G	NCBI36
NG_012494.1:g.409604T>C
NG_012494.2:g.409604T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337414.9:c.589-6391T>C MANE Select	ENSP00000338967.4:n.589-6391T>C
ENST00000657361.1:c.63+4772T>C	ENSP00000499351.1:n.63+4772T>C
ENST00000303025.10:c.-22+4588T>C	ENSP00000302312.6:n.-22+4588T>C
ENST00000337414.8:c.589-6391T>C	ENSP00000338967.4:n.589-6391T>C
ENST00000380717.7:c.97-6391T>C	ENSP00000370093.3:n.97-6391T>C
ENST00000380718.1:c.589-6391T>C	ENSP00000370094.1:n.589-6391T>C
ENST00000380736.5:c.-21-6391T>C	ENSP00000370112.1:n.-21-6391T>C
ENST00000489330.6:n.844-6391T>C
ENST00000495242.5:c.685-6391T>C	ENSP00000435767.1:n.685-6391T>C
NM_001287242.1:c.49-6391T>C	NP_001274171.1:n.49-6391T>C
NM_006125.2:c.589-6391T>C	NP_006116.2:n.589-6391T>C
NM_013423.2:c.-22+4588T>C	NP_038267.1:n.-22+4588T>C
NM_013427.2:c.589-6391T>C	NP_038286.2:n.589-6391T>C
NR_109776.1:n.1558-6391T>C
NM_013427.3:c.589-6391T>C MANE Select	NP_038286.2:n.589-6391T>C
NM_001287242.2:c.49-6391T>C	NP_001274171.1:n.49-6391T>C
NM_006125.3:c.589-6391T>C	NP_006116.2:n.589-6391T>C
NM_013423.3:c.-22+4588T>C	NP_038267.1:n.-22+4588T>C
NR_109776.2:n.1777-6391T>C