Canonical Allele Identifier: CA1069266322

Gene: ARHGAP10

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.148053451T>A , CM000666.2:g.148053451T>A	GRCh38
NC_000004.11:g.148974602T>A , CM000666.1:g.148974602T>A	GRCh37
NC_000004.10:g.149194052T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336498.8:c.2027+6400T>A MANE Select	ENSP00000336923.3:n.2027+6400T>A
ENST00000336498.7:c.2027+6400T>A	ENSP00000336923.3:n.2027+6400T>A
ENST00000506020.5:n.1102+6400T>A
ENST00000506054.5:n.7159+6400T>A
ENST00000507661.1:c.1059+6400T>A
ENST00000513548.1:n.520+6400T>A
NM_024605.3:c.2027+6400T>A	NP_078881.3:n.2027+6400T>A
XM_005263215.2:c.2027+6400T>A	XP_005263272.1:n.2027+6400T>A
XM_011532243.1:c.1673+6400T>A	XP_011530545.1:n.1673+6400T>A
XM_011532244.1:c.1718+6400T>A	XP_011530546.1:n.1718+6400T>A
XM_005263215.3:c.2027+6400T>A	XP_005263272.1:n.2027+6400T>A
XM_017008602.1:c.1751+6400T>A	XP_016864091.1:n.1751+6400T>A
XR_001741324.1:n.2226+6400T>A
NM_024605.4:c.2027+6400T>A MANE Select	NP_078881.3:n.2027+6400T>A