Canonical Allele Identifier: CA788802282

Gene: ARHGAP10

Linked Data

• dbSNP Id: rs1208892483
• MyVariant Identifiers: chr4:g.148884128C>A (hg19) ; chr4:g.147962977C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.147962977C>A , CM000666.2:g.147962977C>A	GRCh38
NC_000004.11:g.148884128C>A , CM000666.1:g.148884128C>A	GRCh37
NC_000004.10:g.149103578C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000336498.8:c.1451-2047C>A MANE Select	ENSP00000336923.3:n.1451-2047C>A
ENST00000336498.7:c.1451-2047C>A	ENSP00000336923.3:n.1451-2047C>A
ENST00000506020.5:n.526-2047C>A
ENST00000506054.5:n.6583-2047C>A
ENST00000507661.1:c.483-2047C>A
NM_024605.3:c.1451-2047C>A	NP_078881.3:n.1451-2047C>A
XM_005263215.2:c.1451-2047C>A	XP_005263272.1:n.1451-2047C>A
XM_011532243.1:c.1097-2047C>A	XP_011530545.1:n.1097-2047C>A
XM_011532244.1:c.1142-2047C>A	XP_011530546.1:n.1142-2047C>A
XM_005263215.3:c.1451-2047C>A	XP_005263272.1:n.1451-2047C>A
XM_017008602.1:c.1175-2047C>A	XP_016864091.1:n.1175-2047C>A
XR_001741324.1:n.1650-2047C>A
NM_024605.4:c.1451-2047C>A MANE Select	NP_078881.3:n.1451-2047C>A