Canonical Allele Identifier: CA1502259367

Gene: ARHGAP10

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.147962960C= , CM000666.2:g.147962960C=	GRCh38
NC_000004.11:g.148884111C= , CM000666.1:g.148884111C=	GRCh37
NC_000004.10:g.149103561C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336498.8:c.1451-2064C= MANE Select	ENSP00000336923.3:n.1451-2064C=
ENST00000336498.7:c.1451-2064C=	ENSP00000336923.3:n.1451-2064C=
ENST00000506020.5:n.526-2064C=
ENST00000506054.5:n.6583-2064C=
ENST00000507661.1:c.483-2064C=
NM_024605.3:c.1451-2064C=	NP_078881.3:n.1451-2064C=
XM_005263215.2:c.1451-2064C=	XP_005263272.1:n.1451-2064C=
XM_011532243.1:c.1097-2064C=	XP_011530545.1:n.1097-2064C=
XM_011532244.1:c.1142-2064C=	XP_011530546.1:n.1142-2064C=
XM_005263215.3:c.1451-2064C=	XP_005263272.1:n.1451-2064C=
XM_017008602.1:c.1175-2064C=	XP_016864091.1:n.1175-2064C=
XR_001741324.1:n.1650-2064C=
NM_024605.4:c.1451-2064C= MANE Select	NP_078881.3:n.1451-2064C=