Canonical Allele Identifier: CA1502259366

Gene: ARHGAP10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.147962958_147962959delinsGC , CM000666.2:g.147962958_147962959delinsGC	GRCh38
NC_000004.11:g.148884109_148884110delinsGC , CM000666.1:g.148884109_148884110delinsGC	GRCh37
NC_000004.10:g.149103559_149103560delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336498.8:c.1451-2066_1451-2065delinsGC MANE Select	ENSP00000336923.3:n.1451-2066_1451-2065delinsGC
ENST00000336498.7:c.1451-2066_1451-2065delinsGC	ENSP00000336923.3:n.1451-2066_1451-2065delinsGC
ENST00000506020.5:n.526-2066_526-2065delinsGC
ENST00000506054.5:n.6583-2066_6583-2065delinsGC
ENST00000507661.1:c.483-2066_483-2065delinsGC
NM_024605.3:c.1451-2066_1451-2065delinsGC	NP_078881.3:n.1451-2066_1451-2065delinsGC
XM_005263215.2:c.1451-2066_1451-2065delinsGC	XP_005263272.1:n.1451-2066_1451-2065delinsGC
XM_011532243.1:c.1097-2066_1097-2065delinsGC	XP_011530545.1:n.1097-2066_1097-2065delinsGC
XM_011532244.1:c.1142-2066_1142-2065delinsGC	XP_011530546.1:n.1142-2066_1142-2065delinsGC
XM_005263215.3:c.1451-2066_1451-2065delinsGC	XP_005263272.1:n.1451-2066_1451-2065delinsGC
XM_017008602.1:c.1175-2066_1175-2065delinsGC	XP_016864091.1:n.1175-2066_1175-2065delinsGC
XR_001741324.1:n.1650-2066_1650-2065delinsGC
NM_024605.4:c.1451-2066_1451-2065delinsGC MANE Select	NP_078881.3:n.1451-2066_1451-2065delinsGC