Canonical Allele Identifier: CA1897165456
Gene: ARHGAP21 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.24596055G= , CM000672.2:g.24596055G= GRCh38
NC_000010.10:g.24884984G= , CM000672.1:g.24884984G= GRCh37
NC_000010.9:g.24924990G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376410.7:c.3448-12C= ENSP00000365592.3:n.3448-12C=
ENST00000396432.7:c.3478-12C= MANE Select ENSP00000379709.2:n.3478-12C=
ENST00000636789.1:c.2839-12C= ENSP00000490396.1:n.2839-12C=
ENST00000638156.1:c.757-12C= ENSP00000489905.1:n.757-12C=
ENST00000680286.1:c.3499-12C= ENSP00000506388.1:n.3499-12C=
ENST00000320481.10:c.1825-12C= ENSP00000365604.5:n.1825-12C=
ENST00000396432.6:c.3478-12C= ENSP00000379709.2:n.3478-12C=
ENST00000486374.5:n.3637C=
ENST00000612832.4:c.1822-12C= ENSP00000480005.1:n.1822-12C=
NM_020824.3:c.3478-12C= NP_065875.3:n.3478-12C=
XM_005252542.2:c.3478-12C= XP_005252599.1:n.3478-12C=
XM_005252544.3:c.3448-12C= XP_005252601.1:n.3448-12C=
XM_011519602.1:c.3580-12C= XP_011517904.1:n.3580-12C=
XM_011519603.1:c.3580-12C= XP_011517905.1:n.3580-12C=
XM_011519604.1:c.3580-12C= XP_011517906.1:n.3580-12C=
XM_011519605.1:c.3550-12C= XP_011517907.1:n.3550-12C=
XM_011519606.1:c.3376-12C= XP_011517908.1:n.3376-12C=
XM_011519607.1:c.3580-12C= XP_011517909.1:n.3580-12C=
XR_242701.3:n.3957-12C=
XR_930513.1:n.4059-12C=
XM_005252542.3:c.3478-12C= XP_005252599.1:n.3478-12C=
XM_005252544.4:c.3448-12C= XP_005252601.1:n.3448-12C=
XM_011519602.2:c.3580-12C= XP_011517904.1:n.3580-12C=
XM_011519603.3:c.3580-12C= XP_011517905.1:n.3580-12C=
XM_011519604.2:c.3580-12C= XP_011517906.1:n.3580-12C=
XM_011519605.2:c.3550-12C= XP_011517907.1:n.3550-12C=
XM_011519606.2:c.3376-12C= XP_011517908.1:n.3376-12C=
XM_011519607.2:c.3580-12C= XP_011517909.1:n.3580-12C=
XM_017016459.2:c.3478-12C= XP_016871948.1:n.3478-12C=
XM_017016460.2:c.3448-12C= XP_016871949.1:n.3448-12C=
XM_017016461.1:c.3448-12C= XP_016871950.1:n.3448-12C=
XM_024448088.1:c.3346-12C= XP_024303856.1:n.3346-12C=
XR_001747160.2:n.4235-12C=
XR_001747161.2:n.4133-12C=
XR_001747162.2:n.3937-12C=
XR_001747163.2:n.4103-12C=
XR_242701.5:n.5718-12C=
XR_930513.3:n.5820-12C=
NM_001367447.1:c.3448-12C= NP_001354376.1:n.3448-12C=
NM_001367448.1:c.3478-12C= NP_001354377.1:n.3478-12C=
NM_001367449.1:c.3184-12C= NP_001354378.1:n.3184-12C=
NM_001367450.1:c.3184-12C= NP_001354379.1:n.3184-12C=
NM_001367451.1:c.3448-12C= NP_001354380.1:n.3448-12C=
NM_001367452.1:c.3007-12C= NP_001354381.1:n.3007-12C=
NM_001367453.1:c.3448-12C= NP_001354382.1:n.3448-12C=
NM_001367454.1:c.3478-12C= NP_001354383.1:n.3478-12C=
NM_001367455.1:c.2839-12C= NP_001354384.1:n.2839-12C=
NM_020824.4:c.3478-12C= MANE Select NP_065875.3:n.3478-12C=
NR_160021.1:n.3923-12C=
NR_160022.1:n.3923-12C=
NR_160023.1:n.4121-12C=
NR_160024.1:n.3064-12C=
NR_160025.1:n.3064-12C=