Canonical Allele Identifier: CA1502222799

Gene: ARHGAP10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.147774805G= , CM000666.2:g.147774805G=	GRCh38
NC_000004.11:g.148695956G= , CM000666.1:g.148695956G=	GRCh37
NC_000004.10:g.148915406G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336498.8:c.154+42350G= MANE Select	ENSP00000336923.3:n.154+42350G=
ENST00000336498.7:c.154+42350G=	ENSP00000336923.3:n.154+42350G=
ENST00000510379.1:n.393+42350G=
NM_024605.3:c.154+42350G=	NP_078881.3:n.154+42350G=
XM_005263215.2:c.154+42350G=	XP_005263272.1:n.154+42350G=
XM_005263217.2:c.154+42350G=	XP_005263274.1:n.154+42350G=
XM_005263215.3:c.154+42350G=	XP_005263272.1:n.154+42350G=
XM_017008602.1:c.-290+42350G=	XP_016864091.1:n.-290+42350G=
XR_001741324.1:n.393+42350G=
NM_024605.4:c.154+42350G= MANE Select	NP_078881.3:n.154+42350G=