Canonical Allele Identifier: CA1502222802

Gene: ARHGAP10

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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